Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:925600-925740 | Common:1; Rare:42 | ||||
chr1:1013379-1013570 | Common:4; Rare:63 | ||||
chr1:1047322-1047686 | Common:6; Rare:143; Clinvar:6; Clinvar (benign):10 | ||||
chr1:1308489-1308664 | Common:8; Rare:94 | ||||
chr1:1320997-1321245 | Common:2; Rare:83 | ||||
chr1:1324580-1325049 | Common:3; Rare:194 | ||||
chr1:1375256-1375592 | Common:6; Rare:97 | ||||
chr1:1399221-1399614 | Common:1; Rare:186 | ||||
chr1:1435598-1435781 | Rare:63 | ||||
chr1:1574529-1574963 | Common:1; Rare:199 | ||||
chr1:1615223-1615507 | Common:3; Rare:120 | ||||
chr1:1658935-1659058 | Common:1; Rare:45 | ||||
chr1:1659148-1659301 | Common:1; Rare:58 | ||||
chr1:1692467-1692537 | Common:2; Rare:11 | ||||
chr1:1724221-1724466 | Common:3; Rare:82 |