| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72664948-72665033 | Rare:10 | ||||
| chr2:73951242-73951502 | Common:1; Rare:44 | ||||
| chr2:73984008-73984147 | Rare:28 | ||||
| chr2:74045362-74045665 | Common:1; Rare:49 | ||||
| chr2:74120082-74120367 | Common:1; Rare:93 | ||||
| chr2:74120550-74120603 | Common:1; Rare:12 | ||||
| chr2:84990782-84991039 | Common:1; Rare:36 | ||||
| chr2:85596478-85596537 | Common:1; Rare:20 | ||||
| chr2:86511020-86511202 | Common:2; Rare:31 | ||||
| chr2:88016545-88016822 | Common:8; Rare:116 | ||||
| chr2:88729309-88729604 | Common:1; Rare:52 | ||||
| chr2:95525731-95525980 | Common:1; Rare:42 | ||||
| chr2:95526702-95526823 | Common:1; Rare:41 | ||||
| chr2:96283640-96283832 | Common:1; Rare:55 | ||||
| chr2:96761690-96761983 | Rare:70; Clinvar:2; Clinvar (pathogenic):2 |