| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489732-31490164 | Common:3; Rare:173 | ||||
| chr22:31496286-31496289 | |||||
| chr22:31496375-31496565 | Common:2; Rare:50 | ||||
| chr22:31630795-31631075 | Common:7; Rare:70 | ||||
| chr22:31638392-31638653 | Common:3; Rare:48 | ||||
| chr22:31662206-31662380 | Common:2; Rare:67 | ||||
| chr22:31749595-31749719 | Rare:30 | ||||
| chr22:31750031-31750330 | Common:3; Rare:87 | ||||
| chr22:31753820-31754112 | Common:1; Rare:103 | ||||
| chr22:32474556-32475059 | Common:5; Rare:168; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:32475170-32475337 | Common:2; Rare:47 | ||||
| chr22:32530195-32530474 | Common:3; Rare:46 | ||||
| chr22:32801485-32801718 | Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:35257333-35257513 | Common:1; Rare:39 | ||||
| chr22:35381266-35381326 | Common:1; Rare:5 |