| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118836005-118836208 | Common:1; Rare:43 | ||||
| chr4:119212355-119212772 | Common:5; Rare:131 | ||||
| chr4:119213124-119213255 | Rare:18 | ||||
| chr4:119538961-119539163 | Common:1; Rare:39 | ||||
| chr4:119542493-119542817 | Common:2; Rare:72 | ||||
| chr4:119627161-119627402 | Common:1; Rare:70 | ||||
| chr4:119627702-119627788 | Rare:16 | ||||
| chr4:119627860-119628179 | Common:3; Rare:63 | ||||
| chr4:119628673-119628943 | Common:4; Rare:110 | ||||
| chr4:120066838-120066972 | Common:4; Rare:30 | ||||
| chr4:120067190-120067275 | Common:1; Rare:16 | ||||
| chr4:121696841-121697181 | Common:5; Rare:94 | ||||
| chr4:121765115-121765212 | Common:1; Rare:32 | ||||
| chr4:121801252-121801405 | Common:2; Rare:48 | ||||
| chr4:122732417-122732785 | Common:3; Rare:115; Clinvar:2; Clinvar (benign):2 |