| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519434-55519916 | Common:2; Rare:155 | ||||
| chr2:55618846-55618932 | Rare:24 | ||||
| chr2:55693821-55693970 | Rare:48; Clinvar (benign):2 | ||||
| chr2:58241306-58241414 | Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60756080-60756323 | Rare:80 | ||||
| chr2:60881315-60881649 | Common:2; Rare:131 | ||||
| chr2:61017200-61017770 | Common:4; Rare:168; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144916-61145165 | Common:3; Rare:83 | ||||
| chr2:61470664-61470982 | Rare:108 | ||||
| chr2:61471069-61471386 | Common:2; Rare:122 | ||||
| chr2:61538315-61538594 | Common:2; Rare:71 | ||||
| chr2:61853958-61854123 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888515-61888743 | Common:1; Rare:96 | ||||
| chr2:62506193-62506331 | Common:1; Rare:45 | ||||
| chr2:63588216-63588546 | Common:1; Rare:101; Clinvar:6 |