| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33993080-33993121 | Rare:13 | ||||
| chr20:36049891-36050163 | Common:1; Rare:61 | ||||
| chr20:36050177-36050237 | Rare:11 | ||||
| chr20:36050246-36050288 | Rare:9 | ||||
| chr20:36050322-36050751 | Common:2; Rare:146 | ||||
| chr20:36050887-36051150 | Common:3; Rare:96 | ||||
| chr20:36548854-36549172 | Common:1; Rare:83 | ||||
| chr20:44180902-44181105 | Rare:32 | ||||
| chr20:44188923-44189049 | Rare:25 | ||||
| chr20:45894708-45894869 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:47317377-47317632 | Common:1; Rare:48 | ||||
| chr20:47352541-47352650 | Rare:21 | ||||
| chr20:47357794-47357908 | Rare:17 | ||||
| chr20:49114824-49115085 | Common:4; Rare:55 | ||||
| chr20:50191312-50191630 | Common:1; Rare:102 |