| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:49154470-49154584 | Common:5; Rare:28; Clinvar (benign):1 | ||||
| chr2:49973990-49974311 | Common:2; Rare:105 | ||||
| chr2:50346758-50347111 | Common:2; Rare:108; Clinvar:6; Clinvar (benign):13 | ||||
| chr2:50347275-50347314 | Rare:15 | ||||
| chr2:50347507-50347611 | Common:1; Rare:38 | ||||
| chr2:50347795-50347948 | Rare:32 | ||||
| chr2:51032014-51032282 | Common:1; Rare:64; Clinvar:3 | ||||
| chr2:51033008-51033238 | Common:1; Rare:55 | ||||
| chr2:53767525-53767889 | Common:5; Rare:126 | ||||
| chr2:53786815-53787232 | Common:1; Rare:156 | ||||
| chr2:53859876-53860105 | Rare:83 | ||||
| chr2:53970761-53971168 | Common:12; Rare:151 | ||||
| chr2:54115469-54115496 | Rare:7 | ||||
| chr2:54115510-54115748 | Common:1; Rare:89 | ||||
| chr2:54115815-54115993 | Common:5; Rare:63 |