| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160954280-160954550 | Rare:61 | ||||
| chr1:161021083-161021559 | Common:5; Rare:129 | ||||
| chr1:161038902-161039035 | Common:1; Rare:47 | ||||
| chr1:161045085-161045352 | Common:1; Rare:50 | ||||
| chr1:161045859-161046108 | Common:1; Rare:70 | ||||
| chr1:161098269-161098402 | Common:1; Rare:22 | ||||
| chr1:161117540-161117650 | Rare:21 | ||||
| chr1:161118001-161118181 | Rare:95 | ||||
| chr1:161132404-161132613 | Rare:66 | ||||
| chr1:161132852-161133167 | Common:1; Rare:58 | ||||
| chr1:161133171-161133296 | Rare:21 | ||||
| chr1:161153681-161154085 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr1:161154114-161154376 | Common:2; Rare:64 | ||||
| chr1:161159365-161159572 | Common:2; Rare:64 | ||||
| chr1:161166249-161166521 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):1 |