| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46296745-46296918 | Rare:57 | ||||
| chr22:46335601-46335760 | Common:2; Rare:68; Clinvar:7; Clinvar (benign):6 | ||||
| chr22:46762512-46762669 | Common:3; Rare:54 | ||||
| chr22:50244986-50245070 | Common:1; Rare:34 | ||||
| chr22:50525531-50525683 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50628128-50628274 | Common:7; Rare:72; Clinvar:2 | ||||
| chr22:50783585-50783877 | Common:2; Rare:97 | ||||
| chr3:197106-197319 | Common:3; Rare:71 | ||||
| chr3:2098595-2098962 | Common:4; Rare:145 | ||||
| chr3:3126775-3127015 | Common:4; Rare:108; Clinvar (benign):4 | ||||
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4493165-4493552 | Rare:129; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:4980397-4980422 | Rare:8 | ||||
| chr3:5187321-5187614 | Common:4; Rare:118 | ||||
| chr3:8501608-8501937 | Common:2; Rare:131 |