| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335652-46335842 | Common:3; Rare:85; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46353541-46353874 | Common:2; Rare:106; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr22:46738026-46738083 | Rare:16 | ||||
| chr22:46738129-46738466 | Common:6; Rare:87 | ||||
| chr22:46762522-46762737 | Common:3; Rare:75 | ||||
| chr22:49918283-49918733 | Common:4; Rare:160; Clinvar (benign):3 | ||||
| chr22:50200856-50201035 | Common:3; Rare:69 | ||||
| chr22:50244949-50245394 | Common:4; Rare:140 | ||||
| chr22:50278112-50278535 | Rare:129 | ||||
| chr22:50326854-50327233 | Common:3; Rare:117 | ||||
| chr22:50343237-50343545 | Common:2; Rare:102 | ||||
| chr22:50456417-50456560 | Common:3; Rare:72 | ||||
| chr22:50505456-50505630 | Common:1; Rare:89 | ||||
| chr22:50506584-50506846 | Common:4; Rare:138 | ||||
| chr22:50525531-50525739 | Common:5; Rare:110; Clinvar:3; Clinvar (benign):2 |