| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101475110-101475167 | Rare:13 | ||||
| chr2:102070288-102070480 | Common:2; Rare:32 | ||||
| chr2:102104385-102104723 | Common:6; Rare:83 | ||||
| chr2:102141305-102141791 | Common:5; Rare:78 | ||||
| chr2:102355668-102355974 | Common:2; Rare:75 | ||||
| chr2:102736821-102736936 | Common:1; Rare:58 | ||||
| chr2:105337471-105337620 | Common:1; Rare:68 | ||||
| chr2:105398965-105399227 | Common:1; Rare:97 | ||||
| chr2:105438478-105438620 | Rare:34 | ||||
| chr2:106194237-106194570 | Common:6; Rare:141 | ||||
| chr2:108449098-108449268 | Rare:68 | ||||
| chr2:108534204-108534528 | Common:7; Rare:133 | ||||
| chr2:108719349-108719558 | Common:2; Rare:93 | ||||
| chr2:110204941-110205064 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110677993-110678248 | Rare:88 |