| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50326900-50327290 | Common:6; Rare:218 | ||||
| chr22:50343174-50343402 | Common:4; Rare:178 | ||||
| chr22:50474993-50475236 | Common:9; Rare:141 | ||||
| chr22:50481251-50482170 | Common:4; Rare:379 | ||||
| chr22:50508195-50508324 | Rare:49 | ||||
| chr22:50525470-50525808 | Common:12; Rare:306; Clinvar:11; Clinvar (benign):10 | ||||
| chr22:50526430-50526550 | Common:3; Rare:126; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr22:50530829-50531701 | Common:7; Rare:518 | ||||
| chr22:50532124-50532244 | Rare:29 | ||||
| chr22:50562780-50563120 | Common:11; Rare:168 | ||||
| chr22:50582180-50582740 | Common:4; Rare:448; Clinvar:14; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr22:50582767-50583176 | Common:18; Rare:286; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:50628076-50628328 | Common:17; Rare:199; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:50783598-50783823 | Common:2; Rare:73 | ||||
| chr3:3126773-3127084 | Common:8; Rare:225; Clinvar (benign):8 |