| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17246591-17247048 | Common:5; Rare:194 | ||||
| chr8:17692257-17692370 | Rare:33 | ||||
| chr8:17922595-17923006 | Common:5; Rare:161 | ||||
| chr8:18084952-18085030 | Rare:14 | ||||
| chr8:22245021-22245452 | Common:2; Rare:154 | ||||
| chr8:23225070-23225231 | Common:1; Rare:38 | ||||
| chr8:23457613-23457771 | Common:3; Rare:62 | ||||
| chr8:23528726-23529053 | Rare:100 | ||||
| chr8:26382971-26383136 | Common:3; Rare:74 | ||||
| chr8:27311226-27311505 | Common:7; Rare:109 | ||||
| chr8:27772565-27772709 | Common:4; Rare:50 | ||||
| chr8:27774381-27774578 | Common:2; Rare:43; Clinvar (benign):1 | ||||
| chr8:28092814-28093175 | Common:4; Rare:98 | ||||
| chr8:28490212-28490433 | Common:1; Rare:42 | ||||
| chr8:28701315-28701639 | Common:3; Rare:111 |