| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102736817-102736974 | Common:1; Rare:76 | ||||
| chr2:105037870-105038117 | Common:3; Rare:90 | ||||
| chr2:105337208-105337606 | Common:5; Rare:140 | ||||
| chr2:105398954-105399175 | Rare:79 | ||||
| chr2:105438478-105438644 | Rare:41 | ||||
| chr2:106194219-106194602 | Common:6; Rare:164 | ||||
| chr2:106887086-106887204 | Rare:39 | ||||
| chr2:106887255-106887314 | Rare:13 | ||||
| chr2:108377850-108378164 | Common:1; Rare:62 | ||||
| chr2:108449071-108449268 | Rare:82 | ||||
| chr2:108534190-108534497 | Common:7; Rare:125 | ||||
| chr2:108719336-108719564 | Common:3; Rare:102; Clinvar (benign):1 | ||||
| chr2:108786676-108786831 | Common:2; Rare:91 | ||||
| chr2:110204934-110205068 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110677975-110678259 | Rare:104 |