| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101262338-101262692 | Common:2; Rare:76 | ||||
| chr2:101308688-101308791 | Rare:39 | ||||
| chr2:102141659-102141837 | Rare:32 | ||||
| chr2:102736856-102736943 | Common:1; Rare:30 | ||||
| chr2:105037894-105038169 | Common:4; Rare:99 | ||||
| chr2:105337448-105337620 | Common:2; Rare:81 | ||||
| chr2:105398987-105399228 | Common:1; Rare:87 | ||||
| chr2:105438181-105438804 | Common:4; Rare:117 | ||||
| chr2:106194243-106194570 | Common:6; Rare:139 | ||||
| chr2:108449098-108449268 | Rare:68 | ||||
| chr2:108534204-108534497 | Common:7; Rare:121 | ||||
| chr2:108719341-108719590 | Common:3; Rare:114; Clinvar (benign):2 | ||||
| chr2:109613846-109614022 | Common:2; Rare:65 | ||||
| chr2:110115802-110115930 | Common:2; Rare:32 | ||||
| chr2:110677998-110678212 | Rare:68 |