| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39883402-39883643 | Common:1; Rare:91; Clinvar (pathogenic):1 | ||||
| chr1:39901998-39902133 | Rare:41 | ||||
| chr1:39954892-39955200 | Common:1; Rare:78 | ||||
| chr1:39955575-39955705 | Common:1; Rare:29 | ||||
| chr1:40039727-40040290 | Common:4; Rare:126 | ||||
| chr1:40040349-40040917 | Common:4; Rare:171 | ||||
| chr1:40041242-40041325 | Rare:15 | ||||
| chr1:40097148-40097386 | Common:2; Rare:98; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr1:40161179-40161499 | Common:1; Rare:112 | ||||
| chr1:40161591-40161745 | Common:1; Rare:42 | ||||
| chr1:40161794-40161822 | Rare:9 | ||||
| chr1:40257661-40257824 | Common:2; Rare:42; Clinvar:1 | ||||
| chr1:40257830-40258315 | Common:4; Rare:128; Clinvar:8; Clinvar (benign):1 | ||||
| chr1:40315346-40315584 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr1:40373524-40373843 | Common:1; Rare:74 |