| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39691394-39691524 | Common:1; Rare:24 | ||||
| chr1:39738724-39738903 | Common:2; Rare:35 | ||||
| chr1:39883441-39883593 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
| chr1:40040455-40040791 | Common:3; Rare:98 | ||||
| chr1:40097235-40097316 | Rare:32; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:40161272-40161402 | Rare:33 | ||||
| chr1:40257877-40258282 | Common:4; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr1:40449998-40450145 | Common:1; Rare:59 | ||||
| chr1:40508662-40508773 | Common:3; Rare:30 | ||||
| chr1:40691495-40691805 | Common:3; Rare:153 | ||||
| chr1:42335157-42335369 | Common:5; Rare:105 | ||||
| chr1:42456010-42456378 | Common:1; Rare:97 | ||||
| chr1:42456446-42456587 | Rare:63 | ||||
| chr1:42658307-42658449 | Common:2; Rare:41 | ||||
| chr1:42767023-42767303 | Common:4; Rare:85 |