| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32179937-32180115 | Rare:53 | ||||
| chr1:32200315-32200664 | Common:1; Rare:72 | ||||
| chr1:32201562-32201698 | Rare:23 | ||||
| chr1:32205331-32205684 | Common:4; Rare:100 | ||||
| chr1:32251188-32251574 | Common:3; Rare:99 | ||||
| chr1:32273847-32274163 | Rare:55 | ||||
| chr1:32291812-32292156 | Common:1; Rare:96 | ||||
| chr1:32394410-32394690 | Common:1; Rare:77 | ||||
| chr1:32650423-32650657 | Common:1; Rare:102 | ||||
| chr1:32650916-32651356 | Common:2; Rare:166 | ||||
| chr1:32651768-32651975 | Rare:47 | ||||
| chr1:32817240-32817717 | Common:1; Rare:130; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:33036817-33037118 | Rare:107; Clinvar (pathogenic):1 | ||||
| chr1:33080994-33081152 | Common:1; Rare:36 | ||||
| chr1:34859709-34859905 | Common:1; Rare:54 |