| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36355527-36355731 | Common:1; Rare:68 | ||||
| chr2:36355745-36356118 | Common:3; Rare:125 | ||||
| chr2:36597577-36597976 | Common:4; Rare:162 | ||||
| chr2:36598056-36598312 | Common:15; Rare:109 | ||||
| chr2:36966071-36966306 | Rare:75 | ||||
| chr2:36966451-36967029 | Common:7; Rare:225 | ||||
| chr2:37083840-37084063 | Common:3; Rare:54 | ||||
| chr2:37084217-37084598 | Common:5; Rare:134 | ||||
| chr2:37156523-37156674 | Common:2; Rare:30 | ||||
| chr2:37156680-37156820 | Common:1; Rare:50 | ||||
| chr2:37156887-37157141 | Common:2; Rare:83 | ||||
| chr2:37196304-37196735 | Common:6; Rare:148 | ||||
| chr2:37197051-37197196 | Rare:34 | ||||
| chr2:37231301-37231383 | Common:1; Rare:39 | ||||
| chr2:37231490-37231823 | Common:6; Rare:179; Clinvar:1; Clinvar (benign):5 |