| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663907-97664261 | Common:1; Rare:108 | ||||
| chr2:98608426-98608665 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr2:99154898-99155050 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr2:99180971-99181231 | Common:2; Rare:76 | ||||
| chr2:101002183-101002324 | Rare:52 | ||||
| chr2:102337016-102337326 | Common:2; Rare:62 | ||||
| chr2:102736865-102736932 | Common:1; Rare:20 | ||||
| chr2:105337459-105337610 | Common:1; Rare:75 | ||||
| chr2:105398973-105399192 | Rare:78 | ||||
| chr2:108449102-108449250 | Rare:49 | ||||
| chr2:108534234-108534502 | Common:6; Rare:113 | ||||
| chr2:108654913-108655045 | Rare:34 | ||||
| chr2:108719414-108719564 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr2:110115773-110115886 | Common:1; Rare:33 | ||||
| chr2:110678007-110678227 | Rare:71 |