| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188293680-188293880 | Rare:74 | ||||
| chr2:189440907-189441685 | Common:20; Rare:1048 | ||||
| chr2:189580028-189580428 | Common:4; Rare:71 | ||||
| chr2:189580422-189580565 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:189580635-189581221 | Common:7; Rare:424; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:189581365-189582245 | Common:14; Rare:318 | ||||
| chr2:189582230-189582429 | Rare:38 | ||||
| chr2:189583326-189583483 | Common:3; Rare:52 | ||||
| chr2:189583436-189583836 | Common:12; Rare:101 | ||||
| chr2:189583742-189584548 | Common:16; Rare:233 | ||||
| chr2:189661348-189661554 | Common:3; Rare:73 | ||||
| chr2:189762369-189763188 | Common:10; Rare:1265 | ||||
| chr2:189763090-189763400 | Common:4; Rare:77 | ||||
| chr2:189763678-189764078 | Common:1; Rare:71 | ||||
| chr2:189783820-189784200 | Common:28; Rare:543; Clinvar:5; Clinvar (benign):12 |