| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47782946-47783185 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:47905512-47905847 | Common:3; Rare:167 | ||||
| chr2:48440631-48440865 | Common:7; Rare:113 | ||||
| chr2:53767559-53767849 | Common:4; Rare:101 | ||||
| chr2:53786842-53787213 | Common:1; Rare:143 | ||||
| chr2:53859948-53860138 | Rare:56 | ||||
| chr2:53970780-53971163 | Common:12; Rare:141 | ||||
| chr2:54330747-54330915 | Common:3; Rare:63 | ||||
| chr2:54558213-54558446 | Common:2; Rare:78 | ||||
| chr2:55050205-55050238 | Rare:8 | ||||
| chr2:55050272-55050416 | Common:1; Rare:56 | ||||
| chr2:55050441-55050894 | Common:7; Rare:135 | ||||
| chr2:55232242-55232872 | Common:5; Rare:200 | ||||
| chr2:55419846-55420120 | Common:4; Rare:107 | ||||
| chr2:55519269-55519786 | Common:1; Rare:157 |