Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189784289-189784543 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190534696-190534853 | Common:1; Rare:53 | ||||
chr2:191014138-191014330 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677854-191678147 | Common:4; Rare:83 | ||||
chr2:197434987-197435227 | Rare:76 | ||||
chr2:197453166-197453477 | Rare:94 | ||||
chr2:197499791-197500427 | Common:2; Rare:241; Clinvar:1; Clinvar (benign):2 | ||||
chr2:197515869-197516089 | Common:1; Rare:87 | ||||
chr2:199911140-199911428 | Rare:101 | ||||
chr2:200306455-200306562 | Common:2; Rare:24 | ||||
chr2:200509907-200510053 | Common:1; Rare:59 | ||||
chr2:200811429-200811572 | Common:1; Rare:51 | ||||
chr2:200864648-200864788 | Rare:55 | ||||
chr2:200889005-200889451 | Common:3; Rare:143 | ||||
chr2:201071621-201072037 | Rare:88 |