| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241314818-241314931 | Common:1; Rare:35 | ||||
| chr2:241314998-241315503 | Common:6; Rare:163 | ||||
| chr2:241315622-241316210 | Common:5; Rare:210 | ||||
| chr2:241356067-241356350 | Common:3; Rare:109 | ||||
| chr2:241508521-241508981 | Common:3; Rare:145 | ||||
| chr2:241617467-241617752 | Common:2; Rare:64 | ||||
| chr2:241617932-241618032 | Common:1; Rare:20 | ||||
| chr2:241636964-241637153 | Rare:74 | ||||
| chr2:241637515-241637735 | Common:1; Rare:124 | ||||
| chr2:241686692-241687145 | Common:4; Rare:148 | ||||
| chr2:241687272-241687342 | Common:1; Rare:19 | ||||
| chr2:241687378-241687395 | |||||
| chr2:241701805-241702131 | Common:1; Rare:119 | ||||
| chr2:241734417-241734729 | Common:8; Rare:130; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:241734849-241734927 | Common:3; Rare:29 |