| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78840731-78841183 | Common:2; Rare:165 | ||||
| chr17:78841406-78841497 | Rare:18 | ||||
| chr17:78979920-78980103 | Common:2; Rare:39 | ||||
| chr17:79009664-79009973 | Common:10; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:79074611-79074831 | Common:2; Rare:44 | ||||
| chr17:79777871-79778227 | Common:1; Rare:160 | ||||
| chr17:79796816-79796949 | Rare:41 | ||||
| chr17:79796969-79797514 | Common:1; Rare:185 | ||||
| chr17:79839420-79839694 | Rare:72 | ||||
| chr17:80101358-80101682 | Common:5; Rare:138; Clinvar (benign):5 | ||||
| chr17:80147059-80147448 | Common:7; Rare:158 | ||||
| chr17:80147677-80147780 | Rare:29 | ||||
| chr17:80219534-80219699 | Rare:31 | ||||
| chr17:80220302-80220438 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80260371-80260509 | Rare:43 |