| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761853-159762077 | Common:4; Rare:114 | ||||
| chr6:159789541-159789984 | Common:4; Rare:149 | ||||
| chr6:160991565-160991804 | Common:3; Rare:74 | ||||
| chr6:161273987-161274156 | Rare:27 | ||||
| chr6:162727707-162728060 | Common:3; Rare:119; Clinvar:3 | ||||
| chr6:163416017-163416169 | Common:2; Rare:45 | ||||
| chr6:166342508-166342681 | Common:3; Rare:69 | ||||
| chr6:166627901-166627947 | Rare:12 | ||||
| chr6:166627950-166628032 | Rare:14 | ||||
| chr6:166956227-166956272 | Rare:6; Clinvar:1 | ||||
| chr6:166956491-166956671 | Common:4; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:166999086-166999410 | Common:1; Rare:111 | ||||
| chr6:167966586-167966777 | Common:2; Rare:34 | ||||
| chr6:168079119-168079344 | Common:4; Rare:50 | ||||
| chr6:169253698-169254091 | Common:1; Rare:70 |