| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78681010-78681097 | Rare:23 | ||||
| chr17:78717017-78717070 | Rare:9 | ||||
| chr17:78736726-78736967 | Common:1; Rare:49 | ||||
| chr17:78782219-78782572 | Common:9; Rare:116 | ||||
| chr17:78840736-78841124 | Common:2; Rare:145 | ||||
| chr17:78979866-78980087 | Common:2; Rare:44 | ||||
| chr17:79009707-79009835 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79777918-79778217 | Common:1; Rare:136 | ||||
| chr17:80035855-80036035 | Common:1; Rare:63 | ||||
| chr17:80036521-80036665 | Common:2; Rare:37; Clinvar (benign):2 | ||||
| chr17:80101334-80101661 | Common:4; Rare:135; Clinvar (benign):4 | ||||
| chr17:80147075-80147389 | Common:7; Rare:130 | ||||
| chr17:80187689-80187804 | Rare:31 | ||||
| chr17:80220297-80220453 | Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415096-80415492 | Common:5; Rare:202 |