| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74774834-74775942 | Common:17; Rare:537 | ||||
| chr17:74776031-74776699 | Common:19; Rare:394 | ||||
| chr17:74872487-74872887 | Common:3; Rare:116 | ||||
| chr17:74872893-74873156 | Common:3; Rare:92; Clinvar (pathogenic):1 | ||||
| chr17:74873267-74873618 | Common:13; Rare:239 | ||||
| chr17:74923196-74923350 | Common:2; Rare:76; Clinvar:2 | ||||
| chr17:74972018-74972350 | Common:4; Rare:135 | ||||
| chr17:74972570-74972956 | Common:7; Rare:229 | ||||
| chr17:74987451-74987703 | Rare:173 | ||||
| chr17:75012383-75012750 | Common:4; Rare:192 | ||||
| chr17:75019873-75021040 | Common:13; Rare:434 | ||||
| chr17:75046848-75047283 | Common:6; Rare:369 | ||||
| chr17:75047446-75047846 | Common:2; Rare:140 | ||||
| chr17:75087532-75088029 | Common:9; Rare:146 | ||||
| chr17:75093050-75093554 | Common:3; Rare:187 |