| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38748341-38748557 | Common:3; Rare:318 | ||||
| chr20:38748710-38749110 | Common:3; Rare:181 | ||||
| chr20:38804837-38805439 | Common:4; Rare:272 | ||||
| chr20:38805460-38805910 | Common:12; Rare:242 | ||||
| chr20:38926025-38927387 | Common:22; Rare:944 | ||||
| chr20:38961399-38961955 | Common:4; Rare:165 | ||||
| chr20:38962031-38962457 | Common:12; Rare:942 | ||||
| chr20:38962550-38962820 | Common:4; Rare:151 | ||||
| chr20:40689114-40689523 | Common:4; Rare:242; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:41028424-41028999 | Common:1; Rare:1088 | ||||
| chr20:41029229-41029629 | Common:1; Rare:127 | ||||
| chr20:41136822-41137244 | Common:3; Rare:349 | ||||
| chr20:41137290-41137680 | Common:5; Rare:319 | ||||
| chr20:41137847-41138247 | Rare:161 | ||||
| chr20:41317080-41317492 | Common:10; Rare:315 |