| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113157241-113157524 | Common:3; Rare:72 | ||||
| chr2:113198986-113199019 | Common:1; Rare:18 | ||||
| chr2:113220116-113220229 | Rare:34; Clinvar:1 | ||||
| chr2:113235473-113235750 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr2:113236871-113236889 | Common:1; Rare:5 | ||||
| chr2:113236891-113236919 | Rare:5 | ||||
| chr2:113236923-113237122 | Common:2; Rare:36 | ||||
| chr2:113241733-113241976 | Common:1; Rare:72 | ||||
| chr2:113437516-113437924 | Common:4; Rare:136 | ||||
| chr2:113627054-113627304 | Common:3; Rare:74 | ||||
| chr2:113756443-113756781 | Common:4; Rare:105 | ||||
| chr2:113889757-113890290 | Common:9; Rare:166 | ||||
| chr2:113890925-113891090 | Rare:40 | ||||
| chr2:115161830-115162232 | Common:3; Rare:126 | ||||
| chr2:118014023-118014243 | Common:2; Rare:117 |