Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1324600-1324802 | Common:2; Rare:113 | ||||
chr1:1358526-1358808 | Common:1; Rare:92 | ||||
chr1:1399306-1399582 | Common:1; Rare:121 | ||||
chr1:1407218-1407399 | Common:1; Rare:83 | ||||
chr1:1435604-1435724 | Rare:43 | ||||
chr1:1574565-1574947 | Common:1; Rare:174 | ||||
chr1:1658920-1659169 | Common:5; Rare:99 | ||||
chr1:2391540-2391923 | Common:2; Rare:140 | ||||
chr1:3624758-3625045 | Common:1; Rare:95 | ||||
chr1:3857168-3857513 | Common:1; Rare:96 | ||||
chr1:3900210-3900406 | Common:12; Rare:94 | ||||
chr1:5992418-5992727 | Common:4; Rare:99; Clinvar:4 | ||||
chr1:7961479-7961787 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026291-8026417 | Rare:53 | ||||
chr1:8878583-8878872 | Rare:153 |