| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119542460-119542837 | Common:2; Rare:82 | ||||
| chr4:119627691-119627788 | Rare:16 | ||||
| chr4:119627840-119628330 | Common:5; Rare:90 | ||||
| chr4:119628602-119628753 | Common:1; Rare:56 | ||||
| chr4:119628824-119629176 | Common:7; Rare:133 | ||||
| chr4:120066784-120066964 | Common:4; Rare:51 | ||||
| chr4:121696854-121697198 | Common:5; Rare:97 | ||||
| chr4:121801092-121801396 | Common:3; Rare:92 | ||||
| chr4:122732436-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122826932-122827220 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr4:122922951-122923118 | Common:2; Rare:48 | ||||
| chr4:123396677-123396874 | Rare:51 | ||||
| chr4:123398280-123398457 | Common:1; Rare:61 | ||||
| chr4:123399368-123399653 | Common:1; Rare:89 | ||||
| chr4:128061000-128061325 | Common:1; Rare:116 |