| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58047074-58047209 | Rare:41 | ||||
| chr2:58241309-58241411 | Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:60550894-60551013 | Rare:33 | ||||
| chr2:60756080-60756283 | Rare:65 | ||||
| chr2:60881315-60881688 | Common:2; Rare:135 | ||||
| chr2:61017429-61017753 | Common:1; Rare:96; Clinvar:2 | ||||
| chr2:61144926-61145164 | Common:3; Rare:79 | ||||
| chr2:61177224-61177472 | Common:5; Rare:111 | ||||
| chr2:61470667-61470987 | Rare:107 | ||||
| chr2:61471257-61471396 | Common:4; Rare:51 | ||||
| chr2:61536504-61536767 | Common:2; Rare:76 | ||||
| chr2:61538211-61538439 | Common:1; Rare:53 | ||||
| chr2:61538512-61538818 | Common:1; Rare:79 | ||||
| chr2:61854023-61854102 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888515-61888743 | Common:1; Rare:96 |