| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451020-178451465 | Common:9; Rare:128; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:178478512-178478747 | Common:1; Rare:75 | ||||
| chr2:178479049-178479174 | Common:1; Rare:24 | ||||
| chr2:178480175-178480622 | Common:3; Rare:129 | ||||
| chr2:178480989-178481093 | Rare:24 | ||||
| chr2:179049663-179049929 | Common:2; Rare:70 | ||||
| chr2:179050034-179050207 | Rare:39 | ||||
| chr2:179264498-179264932 | Common:4; Rare:172 | ||||
| chr2:180006821-180006899 | Common:1; Rare:27 | ||||
| chr2:180007021-180007143 | Rare:29 | ||||
| chr2:180007259-180007451 | Common:1; Rare:50 | ||||
| chr2:180980183-180980830 | Common:4; Rare:198 | ||||
| chr2:180980999-180981092 | Rare:28 | ||||
| chr2:181456745-181456917 | Common:1; Rare:55 | ||||
| chr2:181457174-181457704 | Common:2; Rare:200 |