| ID: 129661700 | ReSE screen-validated silencer GRCh37_chr6:30642736-30642875 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30674959..30675098) | | |
| ID: 127405724 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30650651-30651540 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30682874..30683763) | | |
| ID: 127405723 | H3K27ac hESC enhancer GRCh37_chr6:30640498-30641094 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30672721..30673317) | | |
| ID: 127405722 | H3K4me1 hESC enhancer GRCh37_chr6:30638704-30639302 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30670927..30671525) | | |
| ID: 127405720 | H3K27ac hESC enhancer GRCh37_chr6:30538839-30539400 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30571062..30571623) | | |
| ID: 127405719 | H3K27ac hESC enhancer GRCh37_chr6:30524675-30525239 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30556898..30557462) | | |
| ID: 127405718 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30524110-30524674 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30556333..30556897) | | |
| ID: 127405717 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30523544-30524109 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30555767..30556332) | | |
| ID: 127405716 | H3K4me1 hESC enhancer GRCh37_chr6:30485727-30486226 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30517950..30518449) | | |
| ID: 127405715 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30481847-30482624 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30514070..30514847) | | |
| ID: 127405714 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30457579-30458127 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30489802..30490350) | | |
| ID: 113174988 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30649761-30650650 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30681984..30682873) | | |
| ID: 111082993 | long intergenic non-protein coding RNA 2569 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30516266..30519580) | TCONS_00011283 | |
| ID: 107986587 | ABCF1 divergent transcript [Homo sapiens (human)] | | | |
| ID: 100129192 | MHC class I polypeptide-related sequence C (pseudogene) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30414711..30416636) | PERB11.3 | |
| ID: 100126314 | microRNA 877 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30584332..30584417) | MIRN877, hsa-mir-877, miRNA877, mir-877 | 611619 |
| ID: 170954 | protein phosphatase 1 regulatory subunit 18 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30676389..30688391, complement) | HKMT1098, KIAA1949 | 610990 |
| ID: 80742 | proline rich 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30556709..30563723) | CAT56 | |
| ID: 8449 | DEAH-box helicase 16 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30653127..30673006, complement) | DBP2, DDX16, NMOAS, PRO2014, PRP8, PRPF2, Prp2 | 603405 |
| ID: 3133 | major histocompatibility complex, class I, E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30489509..30494194) | HLA-6.2, QA1 | 143010 |