| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45502553-45502982 | Common:2; Rare:127 | ||||
| chr22:46250257-46250374 | Common:2; Rare:33 | ||||
| chr22:46296760-46296934 | Rare:57 | ||||
| chr22:46762526-46762701 | Common:3; Rare:60 | ||||
| chr22:49918286-49918698 | Common:4; Rare:143; Clinvar (benign):3 | ||||
| chr22:50326915-50327207 | Common:3; Rare:94 | ||||
| chr22:50343188-50343390 | Common:2; Rare:85 | ||||
| chr22:50481468-50481575 | Rare:30 | ||||
| chr22:50582396-50582464 | Rare:31 | ||||
| chr22:50582784-50583124 | Common:7; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628101-50628280 | Common:9; Rare:86; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783598-50783822 | Common:2; Rare:73 | ||||
| chr3:3126810-3126987 | Common:4; Rare:75; Clinvar (benign):2 | ||||
| chr3:4303008-4303427 | Common:2; Rare:118 | ||||
| chr3:5122454-5122562 | Rare:22 |