| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218270935-218271741 | Common:4; Rare:282; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218286617-218287443 | Common:9; Rare:321 | ||||
| chr2:218287742-218288142 | Rare:52 | ||||
| chr2:218289902-218290302 | Common:7; Rare:108 | ||||
| chr2:218290411-218291484 | Common:5; Rare:218 | ||||
| chr2:218292384-218292784 | Common:4; Rare:267 | ||||
| chr2:218316533-218316990 | Common:4; Rare:124 | ||||
| chr2:218322965-218323349 | Common:30; Rare:545 | ||||
| chr2:218323427-218323570 | Common:2; Rare:56 | ||||
| chr2:218356613-218357013 | Common:2; Rare:138 | ||||
| chr2:218397704-218397971 | Common:6; Rare:161 | ||||
| chr2:218397901-218398779 | Common:22; Rare:982 | ||||
| chr2:218398697-218400081 | Common:23; Rare:2287 | ||||
| chr2:218400252-218401330 | Common:77; Rare:1185 | ||||
| chr2:218568254-218568679 | Common:25; Rare:688 |