| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190319719-190319875 | Common:4; Rare:65; Clinvar (benign):5 | ||||
| chr2:190343868-190344031 | Rare:32 | ||||
| chr2:190489560-190489848 | Common:2; Rare:57 | ||||
| chr2:190534631-190534870 | Common:2; Rare:74 | ||||
| chr2:190648709-190648923 | Common:1; Rare:78 | ||||
| chr2:190880588-190880899 | Common:4; Rare:109 | ||||
| chr2:190881014-190881254 | Common:1; Rare:95 | ||||
| chr2:191014109-191014333 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245219-191245611 | Common:4; Rare:127 | ||||
| chr2:191246152-191246344 | Common:1; Rare:50 | ||||
| chr2:191677852-191678234 | Common:4; Rare:107 | ||||
| chr2:191678560-191678621 | Rare:26 | ||||
| chr2:191846722-191846764 | Rare:11 | ||||
| chr2:191846972-191847376 | Rare:74 | ||||
| chr2:192194917-192195054 | Rare:26 |