| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29617158-29617365 | Rare:69 | ||||
| chr17:29618058-29618114 | Rare:17 | ||||
| chr17:29622827-29623038 | Common:3; Rare:79 | ||||
| chr17:29760827-29761013 | Rare:35 | ||||
| chr17:29761061-29761131 | Rare:24 | ||||
| chr17:29761165-29761631 | Common:5; Rare:187 | ||||
| chr17:29929133-29929225 | Rare:22 | ||||
| chr17:29929749-29929946 | Common:1; Rare:55 | ||||
| chr17:29930140-29930338 | Rare:61 | ||||
| chr17:30116599-30117131 | Common:2; Rare:151 | ||||
| chr17:30235676-30235885 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:30235935-30236126 | Rare:48 | ||||
| chr17:30236229-30236298 | Common:1; Rare:9 | ||||
| chr17:30291287-30291435 | Rare:53 | ||||
| chr17:30291903-30292246 | Common:2; Rare:119 |