| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801252-121801411 | Common:2; Rare:50 | ||||
| chr4:121823784-121824052 | Common:4; Rare:66 | ||||
| chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922516-122922707 | Common:3; Rare:86 | ||||
| chr4:122922897-122923123 | Common:2; Rare:57 | ||||
| chr4:127880784-127880967 | Rare:63 | ||||
| chr4:128060979-128061348 | Common:1; Rare:133 | ||||
| chr4:129093468-129093741 | Common:1; Rare:81 | ||||
| chr4:137532456-137532755 | Common:1; Rare:50 | ||||
| chr4:139301215-139301568 | Common:5; Rare:104 | ||||
| chr4:139453777-139454136 | Common:2; Rare:89; Clinvar:9; Clinvar (benign):2 | ||||
| chr4:140373384-140373696 | Common:2; Rare:126 | ||||
| chr4:141220782-141220993 | Rare:74 | ||||
| chr4:144646601-144646697 | Rare:32 | ||||
| chr4:145098141-145098361 | Rare:77 |