Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:138242342-138242642 | Common:1; Rare:63 | ||||
chr4:139301223-139301531 | Common:4; Rare:88 | ||||
chr4:139453774-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
chr4:140373384-140373696 | Common:2; Rare:126 | ||||
chr4:145098146-145098345 | Rare:70 | ||||
chr4:145619207-145619400 | Rare:73 | ||||
chr4:147684133-147684320 | Rare:83 | ||||
chr4:151226361-151226509 | Rare:26 | ||||
chr4:151227753-151228016 | Rare:39 | ||||
chr4:152779762-152780016 | Common:1; Rare:69 | ||||
chr4:158671830-158672139 | Common:4; Rare:82 | ||||
chr4:158672226-158672365 | Rare:32; Clinvar:2 | ||||
chr4:158723315-158723463 | Common:2; Rare:66 | ||||
chr4:169010233-169010368 | Common:1; Rare:44 | ||||
chr4:169620267-169620604 | Common:2; Rare:120 |