| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519831-55519913 | Rare:31 | ||||
| chr2:55618841-55619016 | Common:1; Rare:42 | ||||
| chr2:55693821-55693947 | Rare:45; Clinvar (benign):2 | ||||
| chr2:58046606-58046845 | Rare:73 | ||||
| chr2:61017429-61017771 | Common:1; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144916-61145165 | Common:3; Rare:83 | ||||
| chr2:61470651-61470982 | Rare:111 | ||||
| chr2:61471083-61471392 | Common:4; Rare:119 | ||||
| chr2:61538211-61538439 | Common:1; Rare:53 | ||||
| chr2:61538710-61538855 | Common:1; Rare:46 | ||||
| chr2:61854026-61854223 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888487-61888743 | Common:1; Rare:108 | ||||
| chr2:63588931-63589025 | Rare:35 | ||||
| chr2:63840785-63841154 | Common:2; Rare:113 | ||||
| chr2:63841620-63841954 | Common:2; Rare:111 |