| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207911045-207911129 | Rare:33 | ||||
| chr1:208244260-208244532 | Common:1; Rare:82 | ||||
| chr1:209652395-209652571 | Rare:44; Clinvar:1 | ||||
| chr1:209675257-209675547 | Common:2; Rare:74 | ||||
| chr1:209806008-209806269 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:212035494-212035803 | Common:2; Rare:87 | ||||
| chr1:212432769-212433037 | Rare:74 | ||||
| chr1:212608478-212608761 | Rare:73 | ||||
| chr1:212791759-212791930 | Common:3; Rare:68 | ||||
| chr1:212858089-212858240 | Common:3; Rare:31 | ||||
| chr1:214551560-214551876 | Common:2; Rare:111 | ||||
| chr1:217631020-217631390 | Common:3; Rare:107 | ||||
| chr1:219173786-219173902 | Common:1; Rare:65 | ||||
| chr1:221742041-221742433 | Common:2; Rare:99 | ||||
| chr1:222589859-222590016 | Common:2; Rare:45 |