| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:153887145-153887400 | Common:1; Rare:79 | ||||
| chr7:153887424-153887443 | Rare:4 | ||||
| chr7:153887469-153887731 | Common:2; Rare:60 | ||||
| chr7:155003413-155003512 | Common:3; Rare:54 | ||||
| chr7:155644339-155644886 | Common:6; Rare:175 | ||||
| chr7:156640548-156640791 | Common:2; Rare:114 | ||||
| chr7:156893134-156893383 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:157336790-157337070 | Common:2; Rare:129; Clinvar:1 | ||||
| chr7:157358048-157358350 | Common:1; Rare:86 | ||||
| chr7:158704774-158704975 | Common:1; Rare:71 | ||||
| chr7:158829944-158829969 | Common:1; Rare:9 | ||||
| chr7:158856411-158856750 | Common:7; Rare:117 | ||||
| chr8:232093-232470 | Common:3; Rare:153 | ||||
| chr8:233035-233223 | Common:1; Rare:40 | ||||
| chr8:406717-407018 | Common:4; Rare:143 |