| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189441100-189441504 | Common:2; Rare:119 | ||||
| chr2:189580764-189580896 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784125 | Common:3; Rare:61; Clinvar (benign):1 | ||||
| chr2:189784281-189784560 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190880614-190880882 | Common:4; Rare:92 | ||||
| chr2:191014143-191014333 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677854-191678147 | Common:4; Rare:83 | ||||
| chr2:192194896-192195077 | Rare:39 | ||||
| chr2:196068817-196068921 | Common:1; Rare:28 | ||||
| chr2:196593525-196593620 | Rare:26 | ||||
| chr2:196926670-196926799 | Common:2; Rare:52 | ||||
| chr2:197434980-197435192 | Rare:71 | ||||
| chr2:197453244-197453554 | Rare:104 | ||||
| chr2:197499816-197500453 | Common:1; Rare:248; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199457406-199457710 | Rare:59 |