Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150293730-150293922 | Common:1; Rare:69 | ||||
chr1:150487247-150487473 | Common:3; Rare:63; Clinvar (benign):3 | ||||
chr1:150578985-150579126 | Common:1; Rare:58 | ||||
chr1:150579585-150579901 | Common:10; Rare:99 | ||||
chr1:150629061-150629305 | Rare:73 | ||||
chr1:150629538-150629889 | Common:2; Rare:80 | ||||
chr1:150697097-150697461 | Common:1; Rare:77 | ||||
chr1:150765773-150765894 | Rare:10 | ||||
chr1:150876560-150876869 | Common:5; Rare:115 | ||||
chr1:150926147-150926440 | Rare:89 | ||||
chr1:150961897-150962148 | Rare:45 | ||||
chr1:150974683-150974911 | Common:2; Rare:73 | ||||
chr1:151146606-151146802 | Rare:44 | ||||
chr1:151165856-151166162 | Common:3; Rare:86 | ||||
chr1:151281987-151282339 | Rare:96 |