Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149850803-149851065 | Rare:5 | ||||
chr1:149886640-149887025 | Common:2; Rare:143 | ||||
chr1:149927767-149927869 | Rare:40; Clinvar (benign):3 | ||||
chr1:150293835-150293896 | Rare:21 | ||||
chr1:150321421-150321590 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150629535-150629785 | Rare:53 | ||||
chr1:150982190-150982339 | Common:2; Rare:24 | ||||
chr1:151165889-151166166 | Common:3; Rare:81 | ||||
chr1:151254593-151254774 | Rare:41 | ||||
chr1:151540137-151540313 | Rare:49 | ||||
chr1:151763434-151763702 | Common:3; Rare:101 | ||||
chr1:151790452-151790837 | Common:2; Rare:89 | ||||
chr1:151909421-151909709 | Common:3; Rare:98 | ||||
chr1:153535924-153536089 | Common:1; Rare:36 | ||||
chr1:153545767-153545916 | Rare:26 |