| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066775-120066964 | Common:4; Rare:54 | ||||
| chr4:121696850-121697130 | Common:5; Rare:75 | ||||
| chr4:121801246-121801445 | Common:2; Rare:66 | ||||
| chr4:121823857-121824086 | Common:2; Rare:59 | ||||
| chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922929-122923115 | Common:2; Rare:48 | ||||
| chr4:127880791-127880939 | Rare:50 | ||||
| chr4:128060979-128061325 | Common:1; Rare:125 | ||||
| chr4:128287773-128288057 | Common:3; Rare:107 | ||||
| chr4:128811070-128811317 | Rare:50 | ||||
| chr4:129093475-129093736 | Common:1; Rare:78 | ||||
| chr4:138242334-138242520 | Common:1; Rare:44 | ||||
| chr4:139301291-139301549 | Common:4; Rare:79 | ||||
| chr4:139453773-139454198 | Common:3; Rare:110; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373382-140373701 | Common:2; Rare:129 |