| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41582143-41582327 | Common:1; Rare:40 | ||||
| chr17:41586122-41586248 | Common:3; Rare:17 | ||||
| chr17:41611067-41611511 | Common:1; Rare:158; Clinvar:1 | ||||
| chr17:41620940-41621350 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
| chr17:41651443-41651856 | Common:1; Rare:96 | ||||
| chr17:41654184-41654486 | Common:2; Rare:57 | ||||
| chr17:41655822-41656041 | Common:1; Rare:43 | ||||
| chr17:41656126-41656188 | Common:1; Rare:11 | ||||
| chr17:41768947-41769682 | Common:5; Rare:241; Clinvar:36; Clinvar (benign):26; Clinvar (pathogenic):2 | ||||
| chr17:41784224-41784404 | Common:2; Rare:40 | ||||
| chr17:43315652-43315922 | Common:7; Rare:115 | ||||
| chr17:43388310-43388385 | Rare:15 | ||||
| chr17:45149701-45150106 | Common:1; Rare:82 | ||||
| chr17:45247841-45247963 | Rare:24 | ||||
| chr17:45430912-45431035 | Common:1; Rare:22 |