| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37474317-37474581 | Common:1; Rare:101 | ||||
| chr1:37556809-37557050 | Common:2; Rare:97 | ||||
| chr1:37690502-37690723 | Common:5; Rare:55 | ||||
| chr1:37692141-37692577 | Common:5; Rare:98 | ||||
| chr1:37859573-37859780 | Common:3; Rare:66 | ||||
| chr1:37989949-37990276 | Common:1; Rare:106 | ||||
| chr1:38873301-38873614 | Common:4; Rare:107 | ||||
| chr1:39026237-39026398 | Common:1; Rare:43 | ||||
| chr1:39026593-39026843 | Common:1; Rare:41 | ||||
| chr1:39414094-39414342 | Common:1; Rare:74 | ||||
| chr1:39562131-39562346 | Rare:44 | ||||
| chr1:39883419-39883570 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
| chr1:40040444-40040836 | Common:3; Rare:118 | ||||
| chr1:40161127-40161394 | Common:1; Rare:64 | ||||
| chr1:40257903-40258282 | Common:4; Rare:103; Clinvar:7; Clinvar (benign):1 |