| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:244048643-244048968 | Common:2; Rare:79 | ||||
| chr1:244049013-244049205 | Common:1; Rare:51 | ||||
| chr1:244049264-244049383 | Rare:26 | ||||
| chr1:244451607-244452382 | Common:2; Rare:232 | ||||
| chr1:244461202-244461296 | Common:1; Rare:28 | ||||
| chr1:244461298-244461526 | Common:1; Rare:76 | ||||
| chr1:244652487-244652530 | Common:1; Rare:18 | ||||
| chr1:244652634-244652952 | Common:2; Rare:86 | ||||
| chr1:244653046-244653452 | Common:1; Rare:142 | ||||
| chr1:244653628-244654105 | Common:2; Rare:130 | ||||
| chr1:244862879-244863808 | Common:10; Rare:350; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:244864245-244864825 | Common:1; Rare:221 | ||||
| chr1:244864957-244865172 | Common:1; Rare:53 | ||||
| chr1:244970672-244971204 | Common:5; Rare:168 | ||||
| chr1:245154412-245154652 | Rare:54 |