| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575120-3575358 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423379-9423697 | Rare:96 | ||||
| chr2:9474515-9474594 | Common:6; Rare:44 | ||||
| chr2:9555712-9555879 | Common:2; Rare:54 | ||||
| chr2:9843391-9843501 | Common:5; Rare:26 | ||||
| chr2:10689910-10689997 | Common:2; Rare:30 | ||||
| chr2:12716756-12717082 | Common:1; Rare:91 | ||||
| chr2:17540376-17540739 | Common:2; Rare:92 | ||||
| chr2:17540761-17540798 | Common:1; Rare:3 | ||||
| chr2:17753689-17753917 | Common:3; Rare:77 | ||||
| chr2:18560308-18560550 | Rare:95 | ||||
| chr2:19901667-19901743 | Common:1; Rare:36 | ||||
| chr2:19990079-19990188 | Rare:26 | ||||
| chr2:20446868-20447084 | Common:3; Rare:83 | ||||
| chr2:20651067-20651242 | Rare:51 |