| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084792-18085041 | Common:4; Rare:149; Clinvar (benign):2 | ||||
| chr8:19013572-19013974 | Common:10; Rare:208 | ||||
| chr8:19757864-19757989 | Common:1; Rare:31 | ||||
| chr8:19816960-19817170 | Common:6; Rare:116 | ||||
| chr8:19818040-19818390 | Rare:202 | ||||
| chr8:21919428-21919783 | Common:4; Rare:227 | ||||
| chr8:22023705-22024369 | Common:3; Rare:201 | ||||
| chr8:22025190-22025500 | Common:2; Rare:192 | ||||
| chr8:22033960-22034480 | Common:3; Rare:212 | ||||
| chr8:22053423-22053653 | Common:2; Rare:56 | ||||
| chr8:22059271-22059371 | Rare:26 | ||||
| chr8:22059275-22059432 | Rare:43 | ||||
| chr8:22066360-22066566 | Rare:46 | ||||
| chr8:22066805-22067205 | Common:3; Rare:227 | ||||
| chr8:22089001-22089251 | Common:6; Rare:150 |