| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26033774-26034159 | Common:4; Rare:140 | ||||
| chr2:26244573-26244984 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345812-26346181 | Common:1; Rare:109 | ||||
| chr2:26401863-26401978 | Common:3; Rare:28 | ||||
| chr2:26764212-26764325 | Rare:43 | ||||
| chr2:27032862-27033009 | Rare:57 | ||||
| chr2:27071503-27071874 | Common:1; Rare:110 | ||||
| chr2:27078439-27078858 | Common:4; Rare:103 | ||||
| chr2:27211903-27212095 | Common:3; Rare:69 | ||||
| chr2:27212271-27212383 | Common:2; Rare:55 | ||||
| chr2:27323029-27323160 | Rare:37; Clinvar (benign):1 | ||||
| chr2:27356750-27357071 | Rare:92 | ||||
| chr2:27370249-27370656 | Common:1; Rare:166 | ||||
| chr2:27582833-27583117 | Rare:92 | ||||
| chr2:27628959-27629085 | Common:1; Rare:67 |