| ID: 129661707 | ReSE screen-validated silencer GRCh37_chr6:31759127-31759287 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31791350..31791510) | | |
| ID: 127405846 | H3K4me1 hESC enhancer GRCh37_chr6:31915103-31915602 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31947326..31947825) | | |
| ID: 127405845 | H3K27ac hESC enhancer GRCh37_chr6:31865398-31865992 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31897621..31898215) | | |
| ID: 127405844 | H3K4me1 hESC enhancer GRCh37_chr6:31864618-31865314 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31896841..31897537) | | |
| ID: 127405843 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31838055-31838988 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31870278..31871211) | | |
| ID: 127405842 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31832029-31832653 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31864252..31864876) | | |
| ID: 127405841 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31831405-31832028 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31863628..31864251) | | |
| ID: 127405840 | H3K27ac hESC enhancer GRCh37_chr6:31830779-31831404 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31863002..31863627) | | |
| ID: 127405833 | H3K27ac hESC enhancer GRCh37_chr6:31763127-31763981 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31795350..31796204) | | |
| ID: 127405831 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31707855-31708486 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31740078..31740709) | | |
| ID: 127405830 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31707224-31707854 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31739447..31740077) | | |
| ID: 127405829 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31704508-31705382 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31736731..31737605) | | |
| ID: 126859651 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:31759783-31760982 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31792006..31793205) | | |
| ID: 121132678 | Sharpr-MPRA regulatory regions 3149 and 4553 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31772872..31773186) | | |
| ID: 107986588 | EHMT2 and SLC44A4 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31877808..31884204) | | |
| ID: 105375020 | uncharacterized LOC105375020 [Homo sapiens (human)] | | | |
| ID: 102060414 | C2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31934474..31941724, complement) | | |
| ID: 100532732 | MSH5-SAPCD1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31739948..31764850) | MSH5-C6orf26 | |
| ID: 80737 | von Willebrand factor A domain containing 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31765590..31777328, complement) | C6orf27, G7c, NG37 | 609693 |
| ID: 80736 | solute carrier family 44 member 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31863192..31878997, complement) | C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1 | 606107 |