| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663882-97664332 | Common:2; Rare:257 | ||||
| chr2:97995113-97995256 | Common:2; Rare:36 | ||||
| chr2:97995880-97996002 | Rare:91 | ||||
| chr2:97996140-97996430 | Common:2; Rare:139 | ||||
| chr2:98444768-98445032 | Common:1; Rare:193 | ||||
| chr2:98608325-98608703 | Common:2; Rare:263; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:99141135-99141735 | Common:4; Rare:348 | ||||
| chr2:99141649-99141752 | Rare:28 | ||||
| chr2:99154855-99155116 | Common:4; Rare:164; Clinvar (benign):5 | ||||
| chr2:99180856-99181252 | Common:4; Rare:209 | ||||
| chr2:99181290-99181550 | Rare:104 | ||||
| chr2:99337220-99337516 | Rare:192 | ||||
| chr2:99489913-99490336 | Common:3; Rare:318 | ||||
| chr2:100417200-100417930 | Common:4; Rare:242 | ||||
| chr2:100562687-100563054 | Common:7; Rare:209 |