| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:201283177-201283363 | Common:1; Rare:36 | ||||
| chr1:201283369-201283612 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:201399309-201399682 | Common:1; Rare:137 | ||||
| chr1:201955281-201955520 | Common:1; Rare:65 | ||||
| chr1:202010312-202010629 | Common:4; Rare:72 | ||||
| chr1:202927192-202927343 | Common:4; Rare:69 | ||||
| chr1:203007226-203007442 | Common:2; Rare:86 | ||||
| chr1:203026361-203026530 | Common:3; Rare:59 | ||||
| chr1:205750171-205750408 | Common:3; Rare:51 | ||||
| chr1:206470222-206470496 | Common:4; Rare:46 | ||||
| chr1:206612445-206612654 | Common:5; Rare:56 | ||||
| chr1:206909553-206909665 | Common:2; Rare:26 | ||||
| chr1:207032648-207032954 | Common:5; Rare:53 | ||||
| chr1:207050955-207051083 | Common:1; Rare:59 | ||||
| chr1:207051197-207051479 | Rare:50 |