| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:26111483-26111925 | Common:4; Rare:294 | ||||
| chr1:26112119-26112392 | Rare:155 | ||||
| chr1:26177305-26177635 | Common:6; Rare:164 | ||||
| chr1:26233919-26234314 | Common:6; Rare:214 | ||||
| chr1:26234382-26234513 | Common:2; Rare:46 | ||||
| chr1:26279894-26280199 | Rare:437 | ||||
| chr1:26306525-26306929 | Common:40; Rare:279 | ||||
| chr1:26336390-26336990 | Common:7; Rare:395 | ||||
| chr1:26432025-26432565 | Common:15; Rare:315; Clinvar:6; Clinvar (benign):3 | ||||
| chr1:26471830-26472100 | Common:3; Rare:100 | ||||
| chr1:26472090-26472723 | Common:15; Rare:457 | ||||
| chr1:26472756-26472938 | Common:2; Rare:104 | ||||
| chr1:26472848-26473257 | Common:2; Rare:321 | ||||
| chr1:26529584-26529875 | Common:5; Rare:173 | ||||
| chr1:26531177-26531577 | Common:5; Rare:107 |