| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46575512-46575641 | Rare:33 | ||||
| chr22:46762455-46762693 | Common:3; Rare:90 | ||||
| chr22:50185725-50185953 | Common:4; Rare:95 | ||||
| chr22:50244960-50245086 | Common:2; Rare:50 | ||||
| chr22:50525547-50525685 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532179-50532278 | Rare:29 | ||||
| chr22:50532494-50532698 | Common:2; Rare:52 | ||||
| chr22:50582784-50583126 | Common:7; Rare:107; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628087-50628252 | Common:8; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:196707-196902 | Common:1; Rare:62 | ||||
| chr3:197162-197332 | Rare:56 | ||||
| chr3:2098536-2098962 | Common:4; Rare:165 | ||||
| chr3:3126833-3126984 | Common:4; Rare:64; Clinvar (benign):1 | ||||
| chr3:4303252-4303644 | Common:3; Rare:148 |