| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159789545-159789984 | Common:4; Rare:149 | ||||
| chr6:159790276-159790526 | Common:8; Rare:82 | ||||
| chr6:160991565-160991787 | Common:3; Rare:67 | ||||
| chr6:162727724-162728102 | Common:3; Rare:115; Clinvar:1 | ||||
| chr6:165986597-165986986 | Common:3; Rare:77 | ||||
| chr6:166342508-166342659 | Common:3; Rare:60 | ||||
| chr6:166956525-166956688 | Common:2; Rare:55; Clinvar:3 | ||||
| chr6:166999129-166999448 | Common:2; Rare:108 | ||||
| chr6:167826816-167827123 | Common:2; Rare:173 | ||||
| chr6:169251642-169251935 | Common:4; Rare:46 | ||||
| chr6:169253770-169254103 | Common:1; Rare:59 | ||||
| chr6:169701958-169702176 | Common:2; Rare:103 | ||||
| chr6:169725248-169725613 | Common:1; Rare:81 | ||||
| chr6:169751507-169751661 | Rare:59; Clinvar (benign):2 | ||||
| chr6:170306548-170306816 | Common:2; Rare:88 |