| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40346434-40346550 | Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41620987-41621361 | Common:7; Rare:136 | ||||
| chr22:41832820-41833149 | Common:3; Rare:104 | ||||
| chr22:42614863-42615246 | Common:3; Rare:156 | ||||
| chr22:42649333-42649593 | Common:6; Rare:90 | ||||
| chr22:43955303-43955542 | Common:3; Rare:71 | ||||
| chr22:45163753-45164003 | Common:2; Rare:97 | ||||
| chr22:46053778-46053878 | Rare:36 | ||||
| chr22:46762517-46762669 | Common:3; Rare:52 | ||||
| chr22:50582818-50583136 | Common:5; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50783628-50783859 | Common:1; Rare:66 | ||||
| chr3:3126775-3126984 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr3:9249624-9249742 | Common:1; Rare:34 | ||||
| chr3:9362978-9363088 | Common:1; Rare:42 | ||||
| chr3:9792414-9792504 | Rare:23 |