| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39691381-39691587 | Common:4; Rare:40 | ||||
| chr1:39738746-39739032 | Common:3; Rare:75 | ||||
| chr1:39883440-39883586 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
| chr1:39954982-39955170 | Common:1; Rare:50 | ||||
| chr1:40040444-40040814 | Common:3; Rare:114 | ||||
| chr1:40097190-40097297 | Rare:51; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr1:40161231-40161442 | Common:1; Rare:68 | ||||
| chr1:40257869-40258282 | Common:4; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
| chr1:40374575-40374669 | Common:12; Rare:23 | ||||
| chr1:40449986-40450175 | Common:3; Rare:74 | ||||
| chr1:40508648-40508816 | Common:4; Rare:46 | ||||
| chr1:40531497-40531653 | Rare:38 | ||||
| chr1:40665438-40665816 | Common:1; Rare:88 | ||||
| chr1:40691495-40691874 | Common:3; Rare:169 | ||||
| chr1:40692039-40692247 | Common:1; Rare:65 |