| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:109760344-109760673 | Common:2; Rare:73 | ||||
| chr2:110179628-110179754 | Rare:31; Clinvar (benign):1 | ||||
| chr2:110181023-110181139 | Common:1; Rare:28 | ||||
| chr2:110307211-110307272 | Common:1; Rare:7 | ||||
| chr2:110424768-110424982 | Common:1; Rare:35 | ||||
| chr2:110610808-110611149 | Common:1; Rare:64 | ||||
| chr2:110678813-110678849 | Rare:8 | ||||
| chr2:110681260-110681525 | Common:1; Rare:54 | ||||
| chr2:111607618-111607786 | Common:1; Rare:37 | ||||
| chr2:111682668-111682842 | Rare:50 | ||||
| chr2:112056318-112056513 | Common:1; Rare:38 | ||||
| chr2:112063668-112063832 | Common:1; Rare:23 | ||||
| chr2:112565708-112565843 | Rare:15 | ||||
| chr2:112583523-112583614 | Rare:13 | ||||
| chr2:112719009-112719152 | Common:3; Rare:32 |