| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:86934798-86935058 | Common:2; Rare:96 | ||||
| chr4:87422578-87422640 | Rare:17 | ||||
| chr4:87529059-87529244 | Common:2; Rare:26 | ||||
| chr4:88523698-88523839 | Common:2; Rare:52 | ||||
| chr4:88697798-88698098 | Common:2; Rare:76 | ||||
| chr4:98929101-98929365 | Common:3; Rare:66 | ||||
| chr4:99088708-99088879 | Common:6; Rare:73 | ||||
| chr4:99564004-99564127 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894368-99894575 | Common:1; Rare:81 | ||||
| chr4:99950271-99950499 | Rare:43 | ||||
| chr4:101347599-101347793 | Common:3; Rare:51 | ||||
| chr4:102760922-102761052 | Rare:43; Clinvar:1 | ||||
| chr4:102827492-102827625 | Rare:43 | ||||
| chr4:102827733-102827971 | Common:1; Rare:73 | ||||
| chr4:102827997-102828122 | Rare:45 |