| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118685318-118685455 | Common:2; Rare:43 | ||||
| chr4:118835952-118836232 | Common:1; Rare:64 | ||||
| chr4:119212355-119212751 | Common:4; Rare:121 | ||||
| chr4:119300484-119300949 | Common:2; Rare:202 | ||||
| chr4:120066754-120066904 | Common:1; Rare:48 | ||||
| chr4:121696922-121697130 | Common:4; Rare:56 | ||||
| chr4:121801218-121801429 | Common:2; Rare:78 | ||||
| chr4:121823784-121824116 | Common:4; Rare:82 | ||||
| chr4:122732432-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922929-122923139 | Common:2; Rare:63 | ||||
| chr4:123399527-123399555 | Rare:8 | ||||
| chr4:127782154-127782395 | Common:2; Rare:72 | ||||
| chr4:127880791-127880947 | Rare:53 | ||||
| chr4:128061000-128061325 | Common:1; Rare:116 | ||||
| chr4:129093468-129093741 | Common:1; Rare:81 |