| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98261148-98261490 | Common:1; Rare:111 | ||||
| chr4:98929093-98929354 | Common:3; Rare:68 | ||||
| chr4:98995407-98995773 | Common:6; Rare:130 | ||||
| chr4:99088697-99088884 | Common:6; Rare:83 | ||||
| chr4:99563593-99563816 | Common:2; Rare:71 | ||||
| chr4:99563974-99564165 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894334-99894615 | Common:3; Rare:96 | ||||
| chr4:99950266-99950476 | Rare:40 | ||||
| chr4:100190463-100190580 | Common:2; Rare:26 | ||||
| chr4:101347552-101347840 | Common:4; Rare:84 | ||||
| chr4:102760934-102761029 | Rare:30; Clinvar:1 | ||||
| chr4:102826774-102826982 | Rare:60 | ||||
| chr4:102827099-102827944 | Common:5; Rare:296 | ||||
| chr4:102827960-102828286 | Common:2; Rare:111 | ||||
| chr4:102868813-102869083 | Common:2; Rare:92 |