| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75646539-75646910 | Common:2; Rare:173 | ||||
| chr2:75710504-75710859 | Common:6; Rare:309 | ||||
| chr2:75710863-75711044 | Common:2; Rare:127 | ||||
| chr2:75710990-75711192 | Common:1; Rare:45 | ||||
| chr2:84458383-84459065 | Common:4; Rare:208 | ||||
| chr2:84459194-84459651 | Common:11; Rare:323; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr2:84459792-84460006 | Common:3; Rare:36 | ||||
| chr2:84516210-84516540 | Common:5; Rare:217 | ||||
| chr2:84905429-84906115 | Common:7; Rare:430 | ||||
| chr2:84970520-84971408 | Common:13; Rare:617 | ||||
| chr2:84971494-84972385 | Common:10; Rare:407 | ||||
| chr2:85132810-85133130 | Common:3; Rare:139 | ||||
| chr2:85133100-85133590 | Common:3; Rare:276 | ||||
| chr2:85327902-85328382 | Common:17; Rare:344 | ||||
| chr2:85354415-85354850 | Common:4; Rare:354 |