| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:31296736-31297086 | Common:5; Rare:115 | ||||
| chr1:32650927-32651304 | Common:2; Rare:148 | ||||
| chr1:32817302-32817650 | Rare:88; Clinvar:5 | ||||
| chr1:32901317-32901554 | Common:1; Rare:54 | ||||
| chr1:35192664-35192693 | Rare:9 | ||||
| chr1:37692235-37692589 | Common:5; Rare:83 | ||||
| chr1:40257915-40258264 | Common:4; Rare:94; Clinvar:7 | ||||
| chr1:40508668-40508754 | Common:1; Rare:23 | ||||
| chr1:40692062-40692263 | Common:1; Rare:62 | ||||
| chr1:42335187-42335349 | Common:3; Rare:84 | ||||
| chr1:42658271-42658441 | Common:2; Rare:48 | ||||
| chr1:42767030-42767293 | Common:3; Rare:74 | ||||
| chr1:42846420-42846634 | Common:1; Rare:55 | ||||
| chr1:42958821-42959078 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43358674-43358986 | Common:7; Rare:95 |