| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929022-98929365 | Common:3; Rare:100 | ||||
| chr4:98995497-98995864 | Common:6; Rare:116 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99144293-99144298 | Rare:2 | ||||
| chr4:99435223-99435604 | Common:3; Rare:70 | ||||
| chr4:99563593-99563760 | Common:2; Rare:49 | ||||
| chr4:99563917-99564173 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99816717-99816995 | Common:3; Rare:63 | ||||
| chr4:99894333-99894620 | Common:3; Rare:98 | ||||
| chr4:99946551-99946775 | Rare:83 | ||||
| chr4:99950167-99950527 | Common:1; Rare:96 | ||||
| chr4:101347529-101347854 | Common:5; Rare:95 | ||||
| chr4:102760916-102761091 | Rare:63; Clinvar:1 | ||||
| chr4:102809688-102809872 | Common:2; Rare:41 | ||||
| chr4:102827041-102827902 | Common:8; Rare:304 |