| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101252650-101252901 | Common:5; Rare:85 | ||||
| chr2:102736856-102736951 | Common:1; Rare:36 | ||||
| chr2:105037894-105038106 | Common:3; Rare:73 | ||||
| chr2:105337454-105337626 | Common:1; Rare:79 | ||||
| chr2:105398987-105399169 | Rare:64 | ||||
| chr2:106194243-106194568 | Common:6; Rare:138 | ||||
| chr2:106886769-106886948 | Common:4; Rare:57 | ||||
| chr2:108449104-108449252 | Rare:49 | ||||
| chr2:108534204-108534504 | Common:7; Rare:123 | ||||
| chr2:108621186-108621275 | Rare:8 | ||||
| chr2:108719352-108719619 | Common:3; Rare:117; Clinvar (benign):2 | ||||
| chr2:109613823-109614101 | Common:2; Rare:98 | ||||
| chr2:110204928-110205070 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:111884151-111884247 | Rare:28 | ||||
| chr2:112275392-112275637 | Common:1; Rare:84 |