| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762526-46762661 | Common:3; Rare:44 | ||||
| chr22:50783585-50783859 | Common:2; Rare:91 | ||||
| chr3:3126793-3126990 | Common:4; Rare:83; Clinvar (benign):2 | ||||
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4467231-4467318 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9362971-9363127 | Common:1; Rare:56 | ||||
| chr3:9397521-9397907 | Common:1; Rare:116 | ||||
| chr3:9792369-9792557 | Rare:55 | ||||
| chr3:9792726-9793115 | Common:3; Rare:136 | ||||
| chr3:9933666-9933860 | Common:1; Rare:74 | ||||
| chr3:10026334-10026484 | Rare:42 | ||||
| chr3:10115522-10115739 | Common:3; Rare:80 | ||||
| chr3:10321048-10321263 | Common:2; Rare:91 | ||||
| chr3:11225837-11225976 | Rare:27 | ||||
| chr3:11272247-11272416 | Common:1; Rare:35 |