Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46198338-46198522 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303166-46303303 | Common:1; Rare:53 | ||||
chr1:46303308-46303820 | Common:2; Rare:142 | ||||
chr1:46604233-46604405 | Rare:45 | ||||
chr1:46718561-46718575 | Rare:2 | ||||
chr1:47333611-47334084 | Common:3; Rare:144 | ||||
chr1:50970094-50970278 | Common:1; Rare:33 | ||||
chr1:51236776-51236877 | Rare:28 | ||||
chr1:51519221-51519423 | Common:8; Rare:87 | ||||
chr1:51878685-51878992 | Common:1; Rare:86 | ||||
chr1:52055144-52055261 | Common:1; Rare:24 | ||||
chr1:52056178-52056350 | Rare:48 | ||||
chr1:52366113-52366297 | Common:1; Rare:55 | ||||
chr1:52553456-52553565 | Common:2; Rare:32 | ||||
chr1:52698056-52698188 | Rare:33 |