| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9423393-9423746 | Rare:110 | ||||
| chr2:9555719-9555992 | Common:2; Rare:91 | ||||
| chr2:9630947-9631336 | Common:3; Rare:125 | ||||
| chr2:9843240-9843533 | Common:6; Rare:88 | ||||
| chr2:10689891-10690070 | Common:4; Rare:69 | ||||
| chr2:10812683-10812996 | Common:3; Rare:117 | ||||
| chr2:11466104-11466309 | Common:4; Rare:56 | ||||
| chr2:11746536-11746661 | Common:2; Rare:41; Clinvar:3 | ||||
| chr2:12716756-12717053 | Common:1; Rare:86 | ||||
| chr2:15561298-15561408 | Rare:45 | ||||
| chr2:15940353-15940591 | Rare:58 | ||||
| chr2:17518425-17518653 | Common:2; Rare:62 | ||||
| chr2:17753711-17754177 | Common:4; Rare:146; Clinvar (benign):1 | ||||
| chr2:17800234-17800518 | Common:6; Rare:50 | ||||
| chr2:18560537-18560803 | Rare:87 |