| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105037833-105038110 | Common:3; Rare:97 | ||||
| chr2:105337454-105337624 | Common:1; Rare:79 | ||||
| chr2:105398963-105399258 | Common:1; Rare:106 | ||||
| chr2:106194243-106194593 | Common:6; Rare:145 | ||||
| chr2:106887245-106887423 | Rare:32 | ||||
| chr2:108377894-108377988 | Rare:14 | ||||
| chr2:108449098-108449268 | Rare:68 | ||||
| chr2:108534138-108534502 | Common:7; Rare:148 | ||||
| chr2:108654786-108655056 | Rare:57 | ||||
| chr2:108719383-108719571 | Common:3; Rare:77; Clinvar (benign):2 | ||||
| chr2:110204941-110205058 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:111898267-111898671 | Common:2; Rare:95 | ||||
| chr2:112275394-112275622 | Common:1; Rare:74 | ||||
| chr2:112584410-112584639 | Common:1; Rare:64 | ||||
| chr2:112584772-112584856 | Rare:20 |