| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31723898-31724079 | Rare:37 | ||||
| chr20:32483440-32483791 | Common:1; Rare:57 | ||||
| chr20:32819714-32819987 | Common:3; Rare:96 | ||||
| chr20:33401493-33401589 | Rare:25 | ||||
| chr20:33720242-33720545 | Common:4; Rare:69 | ||||
| chr20:33731912-33732010 | Rare:37 | ||||
| chr20:33994042-33994106 | Rare:23 | ||||
| chr20:34112168-34112441 | Rare:85 | ||||
| chr20:34303339-34303492 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:34516278-34516451 | Common:3; Rare:69 | ||||
| chr20:34558542-34558727 | Common:1; Rare:47 | ||||
| chr20:34677086-34677305 | Rare:54 | ||||
| chr20:34872821-34872905 | Rare:32 | ||||
| chr20:35147280-35147381 | Common:1; Rare:36 | ||||
| chr20:35284559-35284870 | Common:2; Rare:84 |