| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241881753-241881957 | Common:6; Rare:43 | ||||
| chr2:242088413-242088734 | Common:13; Rare:122 | ||||
| chr20:279319-279433 | Common:2; Rare:51 | ||||
| chr20:324456-324605 | Rare:51 | ||||
| chr20:420581-420899 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr20:869426-869569 | Common:1; Rare:22 | ||||
| chr20:1777299-1777421 | Common:3; Rare:29 | ||||
| chr20:1817607-1817885 | Common:3; Rare:42 | ||||
| chr20:1838643-1838769 | Common:2; Rare:30 | ||||
| chr20:1849333-1849457 | Common:1; Rare:19 | ||||
| chr20:2207363-2207460 | Common:1; Rare:26 | ||||
| chr20:2635411-2635630 | Common:2; Rare:38 | ||||
| chr20:2643827-2643953 | Common:1; Rare:17 | ||||
| chr20:2688545-2688694 | Rare:27 | ||||
| chr20:3106765-3106905 | Rare:28 |