| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699494-15699797 | Common:3; Rare:81 | ||||
| chr17:15945030-15945267 | Common:1; Rare:65 | ||||
| chr17:15999590-15999856 | Common:3; Rare:139; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:16215532-16215682 | Common:1; Rare:65 | ||||
| chr17:16215905-16216246 | Common:4; Rare:102 | ||||
| chr17:16217077-16217253 | Rare:56; Clinvar:1 | ||||
| chr17:16380723-16381182 | Common:4; Rare:152 | ||||
| chr17:17237101-17237196 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:17237324-17237693 | Common:7; Rare:91 | ||||
| chr17:17281182-17281368 | Rare:72 | ||||
| chr17:17476871-17477066 | Common:3; Rare:61 | ||||
| chr17:17591587-17591932 | Common:2; Rare:98 | ||||
| chr17:17781890-17782134 | Rare:63 | ||||
| chr17:17823581-17823926 | Common:5; Rare:141 | ||||
| chr17:18039135-18039454 | Common:5; Rare:87; Clinvar (benign):1 |