Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94417946-94418019 | Common:1; Rare:14 | ||||
chr1:94418060-94418499 | Common:3; Rare:152 | ||||
chr1:94418795-94418834 | Rare:15 | ||||
chr1:94541484-94541551 | Rare:10 | ||||
chr1:94541700-94542036 | Common:1; Rare:90 | ||||
chr1:94820147-94820297 | Common:2; Rare:35 | ||||
chr1:94820424-94820702 | Common:4; Rare:73 | ||||
chr1:94925761-94926220 | Common:2; Rare:86 | ||||
chr1:94926905-94927456 | Common:4; Rare:177 | ||||
chr1:94927494-94927744 | Common:1; Rare:48 | ||||
chr1:95072588-95072799 | Rare:64; Clinvar (benign):1 | ||||
chr1:95072878-95073041 | Common:1; Rare:61 | ||||
chr1:95116822-95116933 | Rare:16 | ||||
chr1:95117230-95117431 | Rare:62 | ||||
chr1:95117983-95118006 | Rare:6 |