| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207792191-207792385 | Common:2; Rare:33 | ||||
| chr2:207869918-207870061 | Common:1; Rare:25 | ||||
| chr2:208294510-208294800 | Common:2; Rare:56 | ||||
| chr2:208312102-208312243 | Rare:45 | ||||
| chr2:210003237-210003266 | Rare:7 | ||||
| chr2:210169960-210170043 | Common:1; Rare:16 | ||||
| chr2:210190259-210190570 | Rare:51 | ||||
| chr2:210442593-210442784 | Rare:37 | ||||
| chr2:212953304-212953436 | Common:1; Rare:24 | ||||
| chr2:213022030-213022140 | Rare:25 | ||||
| chr2:213022318-213022453 | Rare:18 | ||||
| chr2:213023017-213023099 | Rare:15 | ||||
| chr2:213066273-213066329 | Rare:14 | ||||
| chr2:213119138-213119302 | Rare:26 | ||||
| chr2:213147546-213147773 | Common:5; Rare:66 |