Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780549-114780745 | Rare:76 | ||||
chr1:115089446-115089737 | Common:3; Rare:97 | ||||
chr1:117060203-117060341 | Common:2; Rare:35 | ||||
chr1:117929591-117929787 | Rare:54 | ||||
chr1:119140647-119140735 | Rare:23 | ||||
chr1:144461625-144461677 | Common:1; Rare:24 | ||||
chr1:145823936-145824251 | Rare:113 | ||||
chr1:145858996-145859163 | Rare:47 | ||||
chr1:145918680-145918978 | Common:2; Rare:63 | ||||
chr1:145927433-145927648 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958217 | Rare:48 | ||||
chr1:145964605-145964742 | Rare:32 | ||||
chr1:145996526-145996813 | Rare:113 | ||||
chr1:147172130-147172252 | Rare:31 | ||||
chr1:147172427-147172793 | Common:1; Rare:95 |