Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151070434-151070863 | Common:6; Rare:234 | ||||
chr1:151070880-151071350 | Common:2; Rare:187 | ||||
chr1:151165793-151166181 | Common:6; Rare:207 | ||||
chr1:151190013-151190311 | Rare:149 | ||||
chr1:151195056-151195486 | Common:4; Rare:168 | ||||
chr1:151198384-151198806 | Common:4; Rare:213 | ||||
chr1:151254620-151254806 | Rare:89 | ||||
chr1:151281225-151281617 | Common:10; Rare:228 | ||||
chr1:151281660-151281800 | Rare:39 | ||||
chr1:151281890-151282353 | Rare:247 | ||||
chr1:151327209-151327457 | Common:3; Rare:105 | ||||
chr1:151327583-151327829 | Common:4; Rare:92 | ||||
chr1:151346828-151347044 | Rare:114 | ||||
chr1:151347176-151347538 | Rare:160 | ||||
chr1:151399430-151399590 | Common:2; Rare:90; Clinvar (pathogenic):2 |