| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190534656-190534882 | Common:1; Rare:73 | ||||
| chr2:190648695-190648923 | Common:1; Rare:84 | ||||
| chr2:191014121-191014340 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245207-191245573 | Common:3; Rare:117 | ||||
| chr2:191246152-191246260 | Rare:40 | ||||
| chr2:191677846-191678207 | Common:4; Rare:101 | ||||
| chr2:191678565-191679010 | Common:1; Rare:150 | ||||
| chr2:191679121-191679266 | Common:2; Rare:39 | ||||
| chr2:195656945-195657266 | Common:2; Rare:85 | ||||
| chr2:196068808-196068909 | Common:1; Rare:24 | ||||
| chr2:196278599-196278744 | Rare:37 | ||||
| chr2:196639551-196639757 | Rare:67 | ||||
| chr2:196799594-196799792 | Common:1; Rare:63 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453233-197453560 | Rare:111 |