| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36951645-36951924 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:37095955-37096287 | Common:3; Rare:103 | ||||
| chr20:37178865-37179177 | Rare:88 | ||||
| chr20:37289577-37289669 | Common:1; Rare:28 | ||||
| chr20:37527834-37528141 | Common:3; Rare:108 | ||||
| chr20:38033416-38033556 | Common:1; Rare:44 | ||||
| chr20:38166433-38166643 | Common:5; Rare:40 | ||||
| chr20:38805632-38805734 | Common:2; Rare:26 | ||||
| chr20:38926188-38926424 | Common:1; Rare:82 | ||||
| chr20:38962097-38962382 | Common:2; Rare:119 | ||||
| chr20:44210710-44211102 | Common:5; Rare:143 | ||||
| chr20:44522007-44522175 | Common:2; Rare:56 | ||||
| chr20:44651687-44651831 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr20:44966348-44966566 | Common:1; Rare:87 | ||||
| chr20:45348415-45348548 | Common:1; Rare:33 |