| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19251515-19251835 | Common:6; Rare:102 | ||||
| chr1:19312072-19312329 | Common:7; Rare:125 | ||||
| chr1:23778338-23778422 | Common:3; Rare:46 | ||||
| chr1:26432095-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:28643036-28643169 | Rare:52 | ||||
| chr1:31296737-31297045 | Common:4; Rare:96 | ||||
| chr1:32221494-32221803 | Common:1; Rare:54 | ||||
| chr1:32817260-32817667 | Rare:110; Clinvar:5 | ||||
| chr1:35557373-35557534 | Common:1; Rare:33 | ||||
| chr1:35557612-35557834 | Common:2; Rare:80 | ||||
| chr1:37474390-37474584 | Common:1; Rare:78 | ||||
| chr1:37808173-37808646 | Common:1; Rare:115 | ||||
| chr1:38859723-38860031 | Rare:111 | ||||
| chr1:40257923-40258258 | Common:4; Rare:87; Clinvar:6 | ||||
| chr1:42766993-42767294 | Common:4; Rare:99; Clinvar (benign):1 |