| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7872232-7872563 | Common:1; Rare:67 | ||||
| chr4:7939688-7940018 | Common:1; Rare:138 | ||||
| chr4:10116415-10117092 | Common:9; Rare:312 | ||||
| chr4:13581071-13581162 | Rare:32 | ||||
| chr4:15003144-15003205 | Common:1; Rare:30 | ||||
| chr4:15681375-15681965 | Common:4; Rare:182 | ||||
| chr4:15702977-15703103 | Common:2; Rare:22 | ||||
| chr4:17614548-17614731 | Common:3; Rare:110 | ||||
| chr4:17810549-17811020 | Common:3; Rare:136 | ||||
| chr4:25160396-25160751 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233847-25234081 | Rare:98 | ||||
| chr4:25914051-25914330 | Common:2; Rare:118 | ||||
| chr4:26320908-26321045 | Rare:49; Clinvar (benign):1 | ||||
| chr4:26857438-26857776 | Common:4; Rare:92 | ||||
| chr4:26860568-26860865 | Common:3; Rare:103 |