| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190648783-190648916 | Rare:49 | ||||
| chr2:191014124-191014333 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245555 | Common:3; Rare:104 | ||||
| chr2:191246159-191246305 | Common:1; Rare:42 | ||||
| chr2:191677833-191678211 | Common:4; Rare:106 | ||||
| chr2:191678747-191679007 | Common:1; Rare:82 | ||||
| chr2:196799618-196799782 | Common:1; Rare:45 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453171-197453477 | Rare:93 | ||||
| chr2:197499789-197500725 | Common:2; Rare:329; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515962-197516095 | Rare:53 | ||||
| chr2:197705232-197705390 | Common:1; Rare:60 | ||||
| chr2:199911104-199911357 | Rare:74 | ||||
| chr2:200306420-200306566 | Common:2; Rare:34 | ||||
| chr2:200510040-200510125 | Rare:27 |