| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:77979046-77979185 | Common:2; Rare:42 | ||||
| chr1:78004552-78004873 | Common:3; Rare:80 | ||||
| chr1:78490907-78491078 | Common:1; Rare:34 | ||||
| chr1:84077904-84078124 | Common:1; Rare:80 | ||||
| chr1:84479202-84479294 | Common:2; Rare:46 | ||||
| chr1:84690418-84690721 | Rare:99 | ||||
| chr1:85048433-85048617 | Common:2; Rare:40 | ||||
| chr1:85276480-85276570 | Rare:29 | ||||
| chr1:85276623-85276841 | Common:2; Rare:55 | ||||
| chr1:86914323-86914632 | Common:1; Rare:78 | ||||
| chr1:88684027-88684349 | Common:3; Rare:92 | ||||
| chr1:89994981-89995170 | Common:2; Rare:75 | ||||
| chr1:91021963-91022152 | Rare:54 | ||||
| chr1:92298945-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92831871-92832113 | Common:1; Rare:109; Clinvar:6; Clinvar (benign):5 |