Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150487270-150487445 | Common:3; Rare:41; Clinvar (benign):3 | ||||
chr1:150549555-150549795 | Common:2; Rare:40 | ||||
chr1:150557701-150558031 | Common:4; Rare:100; Clinvar:3 | ||||
chr1:150578247-150578719 | Common:2; Rare:142 | ||||
chr1:150579037-150579271 | Rare:101 | ||||
chr1:150579553-150579920 | Common:12; Rare:122 | ||||
chr1:150629119-150629380 | Common:1; Rare:75 | ||||
chr1:150629426-150629825 | Rare:91 | ||||
chr1:150876547-150876981 | Common:5; Rare:153 | ||||
chr1:150926240-150926448 | Rare:59 | ||||
chr1:150974645-150974883 | Common:2; Rare:69 | ||||
chr1:151006808-151006921 | Rare:25 | ||||
chr1:151070356-151070799 | Common:4; Rare:127 | ||||
chr1:151146602-151146827 | Common:1; Rare:56 | ||||
chr1:151156415-151156695 | Rare:49 |