Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109656028-109656151 | Common:2; Rare:40 | ||||
chr1:109656266-109656362 | Rare:27 | ||||
chr1:109984962-109985168 | Rare:73 | ||||
chr1:110339143-110339491 | Common:2; Rare:110 | ||||
chr1:110407367-110407430 | Rare:21 | ||||
chr1:110407550-110407805 | Common:2; Rare:113 | ||||
chr1:110963624-110963672 | Rare:16 | ||||
chr1:110963707-110963978 | Rare:82 | ||||
chr1:111139594-111139881 | Common:1; Rare:56 | ||||
chr1:111140008-111140306 | Common:3; Rare:101 | ||||
chr1:111755481-111755749 | Common:3; Rare:96 | ||||
chr1:112396000-112396275 | Common:1; Rare:85 | ||||
chr1:112619662-112619746 | Rare:27 | ||||
chr1:112619748-112619878 | Common:2; Rare:52 | ||||
chr1:112956029-112956341 | Common:4; Rare:109; Clinvar:11; Clinvar (benign):3 |