| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44167740-44168070 | Common:4; Rare:118 | ||||
| chr2:44168106-44168249 | Common:1; Rare:49 | ||||
| chr2:44168263-44168453 | Common:1; Rare:44 | ||||
| chr2:44168465-44168980 | Common:1; Rare:161 | ||||
| chr2:44361445-44362074 | Common:4; Rare:209 | ||||
| chr2:44362084-44362343 | Rare:75 | ||||
| chr2:44362512-44362595 | Rare:20 | ||||
| chr2:44362602-44362614 | |||||
| chr2:45009380-45009682 | Common:1; Rare:100 | ||||
| chr2:45611156-45611463 | Common:1; Rare:107 | ||||
| chr2:45612311-45612584 | Common:3; Rare:62 | ||||
| chr2:45650949-45651286 | Common:3; Rare:96 | ||||
| chr2:46297079-46297436 | Common:6; Rare:138 | ||||
| chr2:46297636-46297822 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:46335147-46335497 | Rare:63 |