| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191677856-191678147 | Common:4; Rare:82 | ||||
| chr2:192194870-192195075 | Rare:48 | ||||
| chr2:195656852-195657273 | Common:2; Rare:115 | ||||
| chr2:196068797-196068921 | Common:1; Rare:33 | ||||
| chr2:196592682-196592946 | Common:1; Rare:79 | ||||
| chr2:196593525-196593712 | Common:1; Rare:51 | ||||
| chr2:196593746-196593798 | Rare:14 | ||||
| chr2:196799603-196799775 | Common:1; Rare:54 | ||||
| chr2:196926678-196926828 | Common:2; Rare:65 | ||||
| chr2:197434970-197435176 | Rare:70 | ||||
| chr2:197453233-197453584 | Rare:125 | ||||
| chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515934-197516107 | Rare:71 | ||||
| chr2:199455538-199455694 | Rare:30 | ||||
| chr2:199457328-199457752 | Rare:74 |