| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929007-98929506 | Common:3; Rare:129 | ||||
| chr4:98995212-98995823 | Common:10; Rare:193 | ||||
| chr4:98995870-98996054 | Rare:63 | ||||
| chr4:99088248-99088365 | Rare:19 | ||||
| chr4:99088600-99088978 | Common:9; Rare:160 | ||||
| chr4:99089081-99089138 | Common:1; Rare:8 | ||||
| chr4:99563501-99563839 | Common:2; Rare:103 | ||||
| chr4:99563995-99564161 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99574577-99574825 | Common:1; Rare:52 | ||||
| chr4:99816544-99816964 | Common:3; Rare:85 | ||||
| chr4:99894330-99894676 | Common:3; Rare:111 | ||||
| chr4:99946449-99946865 | Rare:148 | ||||
| chr4:99950193-99950775 | Common:2; Rare:161 | ||||
| chr4:101347498-101347881 | Common:5; Rare:110 | ||||
| chr4:101348008-101348184 | Rare:48 |