| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96638292-96638467 | Common:1; Rare:44 | ||||
| chr2:97589697-97589928 | Common:6; Rare:64 | ||||
| chr2:97645811-97646186 | Common:3; Rare:112 | ||||
| chr2:97663901-97664261 | Common:1; Rare:110 | ||||
| chr2:98608373-98608636 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:99154883-99155031 | Common:1; Rare:59 | ||||
| chr2:99180977-99181226 | Common:2; Rare:73 | ||||
| chr2:99337209-99337500 | Rare:99 | ||||
| chr2:101002183-101002318 | Rare:51 | ||||
| chr2:101252650-101252907 | Common:5; Rare:86 | ||||
| chr2:102141628-102141791 | Common:1; Rare:27 | ||||
| chr2:102355697-102355838 | Common:1; Rare:41 | ||||
| chr2:102736826-102736932 | Common:1; Rare:52 | ||||
| chr2:105092148-105092470 | Common:1; Rare:60 | ||||
| chr2:105337454-105337606 | Common:1; Rare:76 |