| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101474994-101475089 | Common:1; Rare:18 | ||||
| chr2:101475099-101475176 | Rare:16 | ||||
| chr2:102736856-102736936 | Common:1; Rare:27 | ||||
| chr2:105037845-105038106 | Common:3; Rare:91 | ||||
| chr2:105337279-105337606 | Common:5; Rare:123 | ||||
| chr2:105396665-105396947 | Common:4; Rare:70 | ||||
| chr2:105396957-105397254 | Common:6; Rare:75 | ||||
| chr2:105398929-105399168 | Common:1; Rare:85 | ||||
| chr2:106194243-106194568 | Common:6; Rare:138 | ||||
| chr2:108449097-108449252 | Rare:53 | ||||
| chr2:108533892-108533970 | Rare:25 | ||||
| chr2:108534199-108534568 | Common:8; Rare:140 | ||||
| chr2:108719365-108719564 | Common:3; Rare:82; Clinvar (benign):1 | ||||
| chr2:110677993-110678252 | Rare:89 | ||||
| chr2:111884117-111884266 | Rare:44 |