| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158644704-158644933 | Common:2; Rare:89 | ||||
| chr6:158649841-158650066 | Common:1; Rare:41 | ||||
| chr6:159000164-159000301 | Rare:33 | ||||
| chr6:159693146-159693414 | Common:4; Rare:93 | ||||
| chr6:159726933-159727185 | Common:1; Rare:94 | ||||
| chr6:159727353-159727701 | Common:5; Rare:142 | ||||
| chr6:159789538-159789952 | Common:4; Rare:136 | ||||
| chr6:160991557-160991789 | Common:3; Rare:67 | ||||
| chr6:162726864-162727132 | Common:3; Rare:53 | ||||
| chr6:162727746-162728063 | Common:3; Rare:86; Clinvar:1 | ||||
| chr6:166342508-166342648 | Common:3; Rare:54 | ||||
| chr6:166999074-166999418 | Common:1; Rare:116 | ||||
| chr6:169701993-169702138 | Common:1; Rare:57 | ||||
| chr6:169751585-169751660 | Rare:34; Clinvar (benign):2 | ||||
| chr6:170306604-170306830 | Common:3; Rare:66 |