| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80363038-80363112 | Rare:23 | ||||
| chr17:80415087-80415189 | Common:1; Rare:67 | ||||
| chr17:80544683-80544902 | Common:2; Rare:57 | ||||
| chr17:80991786-80991938 | Common:1; Rare:57 | ||||
| chr17:81083236-81083514 | Common:1; Rare:79 | ||||
| chr17:81239048-81239311 | Common:2; Rare:88 | ||||
| chr17:81294850-81294942 | Common:1; Rare:30 | ||||
| chr17:81512720-81513159 | Common:7; Rare:221; Clinvar (benign):14 | ||||
| chr17:81666544-81666769 | Common:1; Rare:102 | ||||
| chr17:81683721-81684069 | Common:4; Rare:176 | ||||
| chr17:81703286-81703575 | Common:2; Rare:86; Clinvar (benign):2 | ||||
| chr17:81803839-81804195 | Common:1; Rare:78 | ||||
| chr17:81804723-81804839 | Common:1; Rare:28 | ||||
| chr17:81833243-81833371 | Rare:55 |