| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196776674-196777074 | Common:2; Rare:114 | ||||
| chr2:196799562-196799827 | Common:4; Rare:194 | ||||
| chr2:196926604-196927420 | Common:11; Rare:450 | ||||
| chr2:197310145-197310580 | Common:6; Rare:179 | ||||
| chr2:197310572-197311348 | Common:6; Rare:401 | ||||
| chr2:197434963-197435356 | Rare:296 | ||||
| chr2:197453071-197453663 | Rare:502 | ||||
| chr2:197453774-197454038 | Rare:150 | ||||
| chr2:197499739-197500587 | Common:6; Rare:819; Clinvar:3; Clinvar (benign):8 | ||||
| chr2:197515717-197516213 | Common:4; Rare:368 | ||||
| chr2:197516430-197516910 | Common:5; Rare:165 | ||||
| chr2:197705131-197705531 | Common:9; Rare:447; Clinvar:3; Clinvar (benign):10 | ||||
| chr2:197804407-197804648 | Rare:106 | ||||
| chr2:199457400-199457827 | Common:1; Rare:210 | ||||
| chr2:199457930-199458269 | Common:1; Rare:56 |