| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158611514-158611603 | Common:1; Rare:18 | ||||
| chr6:158771242-158771699 | Common:2; Rare:135 | ||||
| chr6:158776406-158776781 | Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:158869682-158870047 | Common:2; Rare:100 | ||||
| chr6:159463276-159463405 | Rare:27 | ||||
| chr6:159761329-159761492 | Common:1; Rare:40 | ||||
| chr6:159782744-159782942 | Common:2; Rare:49 | ||||
| chr6:160520224-160520648 | Common:9; Rare:132 | ||||
| chr6:160926227-160926324 | Rare:21 | ||||
| chr6:161140172-161140372 | Common:1; Rare:40 | ||||
| chr6:162439578-162439883 | Common:7; Rare:65 | ||||
| chr6:162810012-162810147 | Common:2; Rare:23 | ||||
| chr6:163033872-163033981 | Common:2; Rare:19 | ||||
| chr6:163054134-163054313 | Common:2; Rare:36 | ||||
| chr6:163187745-163187786 | Rare:9 |