| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161154151-161154317 | Common:1; Rare:43 | ||||
| chr1:161159363-161159580 | Common:2; Rare:70 | ||||
| chr1:161159837-161159996 | Common:1; Rare:36 | ||||
| chr1:161166220-161166516 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161166644-161166770 | Rare:25 | ||||
| chr1:161177229-161177299 | Rare:23 | ||||
| chr1:161177418-161177773 | Common:1; Rare:98 | ||||
| chr1:161196966-161197114 | Rare:18 | ||||
| chr1:161197267-161197389 | Common:1; Rare:25 | ||||
| chr1:161198857-161199336 | Rare:86 | ||||
| chr1:161199707-161199775 | Common:1; Rare:8 | ||||
| chr1:161202028-161202490 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):10 | ||||
| chr1:161202602-161202741 | Common:2; Rare:27 | ||||
| chr1:161225623-161226126 | Common:10; Rare:89 | ||||
| chr1:161226468-161226644 | Rare:60 |