| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92962485-92962609 | Common:3; Rare:21 | ||||
| chr1:92995520-92996010 | Common:2; Rare:88 | ||||
| chr1:93446906-93447019 | Rare:20 | ||||
| chr1:93449100-93449640 | Common:3; Rare:168 | ||||
| chr1:93582850-93583366 | Common:3; Rare:316 | ||||
| chr1:93597810-93598090 | Common:1; Rare:39 | ||||
| chr1:93616697-93616916 | Rare:39 | ||||
| chr1:93617810-93618100 | Common:4; Rare:36 | ||||
| chr1:93638430-93638760 | Common:2; Rare:59 | ||||
| chr1:93638950-93639520 | Common:4; Rare:99 | ||||
| chr1:93778546-93779219 | Common:7; Rare:199 | ||||
| chr1:93779756-93780103 | Common:1; Rare:75 | ||||
| chr1:93846247-93846526 | Common:2; Rare:166 | ||||
| chr1:94044380-94044870 | Common:3; Rare:116; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr1:94064068-94064468 | Common:12; Rare:134 |