| ID: 127405710 | NANOG-H3K4me1 hESC enhancer GRCh37_chr6:30292740-30293383 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30324963..30325606) | | |
| ID: 127405709 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30181514-30182402 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30213737..30214625) | | |
| ID: 127405708 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30175183-30176130 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30207406..30208353) | | |
| ID: 126859642 | BRD4-independent group 4 enhancer GRCh37_chr6:30296621-30297820 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30328844..30330043) | | |
| ID: 414778 | HLA complex group 17 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30234039..30326134, complement) | HCG18, LINC00046, NCRNA00046 | |
| ID: 414777 | HLA complex group 18 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30287397..30327156, complement) | | |
| ID: 404024 | tripartite motif containing 26B, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30238301..30242279) | TRIM26P, TRIM26P1 | |
| ID: 202658 | TRIM39-RPP21 readthrough [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30329311..30346858) | TRIM39R | |
| ID: 56658 | tripartite motif containing 39 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30326469..30343729) | RNF23, TFPB, TRIM39 | 605700 |
| ID: 7726 | tripartite motif containing 26 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30184455..30213406, complement) | AFP, RNF95, ZNF173 | 600830 |
| ID: 3139 | major histocompatibility complex, class I, L (pseudogene) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30259562..30266951) | HLA-92, HLA92, HLAL | |