| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563981-99564154 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894357-99894593 | Common:2; Rare:86 | ||||
| chr4:99946564-99946992 | Common:1; Rare:134 | ||||
| chr4:102760927-102761052 | Rare:39; Clinvar:1 | ||||
| chr4:102826779-102826985 | Rare:60 | ||||
| chr4:102827148-102827421 | Common:1; Rare:94 | ||||
| chr4:102827465-102827884 | Common:4; Rare:140 | ||||
| chr4:102827975-102828151 | Common:1; Rare:63 | ||||
| chr4:102868854-102869075 | Common:2; Rare:76 | ||||
| chr4:103076308-103076559 | Common:1; Rare:80 | ||||
| chr4:105552359-105552650 | Rare:44 | ||||
| chr4:105708636-105708843 | Common:1; Rare:68 | ||||
| chr4:105895357-105895521 | Rare:46 | ||||
| chr4:106316174-106316604 | Common:5; Rare:136 | ||||
| chr4:107720193-107720522 | Common:7; Rare:130 |