| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119627986-119628097 | Rare:27 | ||||
| chr4:119628787-119629106 | Common:8; Rare:131 | ||||
| chr4:120066422-120066464 | Rare:7 | ||||
| chr4:120066748-120066960 | Common:3; Rare:65 | ||||
| chr4:121696862-121697130 | Common:5; Rare:73 | ||||
| chr4:121801224-121801396 | Common:2; Rare:60 | ||||
| chr4:121823779-121824076 | Common:4; Rare:71 | ||||
| chr4:121870375-121870624 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr4:122732417-122732834 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922897-122923137 | Common:2; Rare:67 | ||||
| chr4:127880797-127880934 | Rare:45 | ||||
| chr4:128060994-128061329 | Common:1; Rare:118 | ||||
| chr4:129093452-129093736 | Common:1; Rare:81 | ||||
| chr4:133149103-133149294 | Common:2; Rare:55 | ||||
| chr4:137532368-137532755 | Common:3; Rare:68 |