| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159789427-159790037 | Common:5; Rare:212 | ||||
| chr6:159790244-159790569 | Common:8; Rare:117 | ||||
| chr6:159790782-159790981 | Rare:63 | ||||
| chr6:160991663-160991819 | Common:1; Rare:57 | ||||
| chr6:161273993-161274164 | Rare:29 | ||||
| chr6:162727711-162727974 | Rare:90; Clinvar:2 | ||||
| chr6:165986139-165986305 | Common:1; Rare:31 | ||||
| chr6:165986590-165986989 | Common:3; Rare:77 | ||||
| chr6:166167640-166168007 | Common:2; Rare:92 | ||||
| chr6:166168326-166168776 | Common:1; Rare:98 | ||||
| chr6:166342508-166342681 | Common:3; Rare:69 | ||||
| chr6:166956539-166956676 | Common:2; Rare:48; Clinvar:3 | ||||
| chr6:166999035-166999454 | Common:2; Rare:147 | ||||
| chr6:169701954-169702351 | Common:5; Rare:168 | ||||
| chr6:169751459-169751648 | Common:2; Rare:83; Clinvar (benign):2 |