| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105708646-105708827 | Rare:57 | ||||
| chr4:106316185-106316584 | Common:5; Rare:128 | ||||
| chr4:107720181-107720505 | Common:7; Rare:130 | ||||
| chr4:107989679-107989930 | Common:6; Rare:114; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:109730063-109730246 | Common:2; Rare:46 | ||||
| chr4:109815407-109815544 | Common:1; Rare:39 | ||||
| chr4:112285823-112285961 | Rare:41 | ||||
| chr4:112636869-112637181 | Rare:86 | ||||
| chr4:113979611-113979842 | Common:6; Rare:54 | ||||
| chr4:118685319-118685450 | Common:2; Rare:41 | ||||
| chr4:118836060-118836218 | Rare:35 | ||||
| chr4:119628773-119629106 | Common:8; Rare:138 | ||||
| chr4:120066748-120066955 | Common:3; Rare:65 | ||||
| chr4:121696862-121697118 | Common:5; Rare:70 |