| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119212345-119212779 | Common:8; Rare:235 | ||||
| chr4:119212910-119213430 | Common:2; Rare:135 | ||||
| chr4:119300299-119301107 | Common:5; Rare:492 | ||||
| chr4:120066421-120066522 | Rare:25 | ||||
| chr4:120066747-120067004 | Common:9; Rare:144 | ||||
| chr4:120922673-120922795 | Rare:27; Clinvar:2 | ||||
| chr4:121696880-121697199 | Common:10; Rare:162 | ||||
| chr4:121801215-121801473 | Common:4; Rare:173; Clinvar (pathogenic):1 | ||||
| chr4:121823775-121824122 | Common:8; Rare:167 | ||||
| chr4:121870413-121870655 | Common:2; Rare:107; Clinvar (benign):2 | ||||
| chr4:122152233-122152531 | Common:4; Rare:171 | ||||
| chr4:122732400-122732800 | Common:6; Rare:247; Clinvar:6; Clinvar (benign):4 | ||||
| chr4:122826578-122826895 | Common:2; Rare:118 | ||||
| chr4:122922545-122922855 | Common:3; Rare:111 | ||||
| chr4:122922933-122923184 | Common:3; Rare:140; Clinvar:2; Clinvar (pathogenic):2 |