| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931865-7932241 | Common:5; Rare:100 | ||||
| chr17:8295350-8295538 | Common:1; Rare:49 | ||||
| chr17:9576558-9576663 | Common:1; Rare:29 | ||||
| chr17:10697504-10697648 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14069463-14069529 | Common:1; Rare:22; Clinvar (benign):2 | ||||
| chr17:14300775-14301133 | Common:3; Rare:95 | ||||
| chr17:15999527-15999851 | Common:3; Rare:161; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:16215525-16215657 | Common:1; Rare:53 | ||||
| chr17:16216896-16217233 | Rare:80; Clinvar:1 | ||||
| chr17:17591657-17591718 | Rare:14 | ||||
| chr17:18039146-18039422 | Common:4; Rare:72; Clinvar (benign):1 | ||||
| chr17:18314913-18315332 | Common:1; Rare:119 | ||||
| chr17:19377914-19378030 | Common:1; Rare:24 | ||||
| chr17:19378163-19378583 | Common:2; Rare:98 | ||||
| chr17:21214123-21214344 | Common:2; Rare:99 |