| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:159924592-159924801 | Rare:44 | ||||
| chr1:159925444-159925688 | Common:1; Rare:62 | ||||
| chr1:159945594-159945882 | Common:2; Rare:71 | ||||
| chr1:159945954-159946124 | Rare:40 | ||||
| chr1:160031773-160032173 | Common:3; Rare:101 | ||||
| chr1:160098826-160099127 | Common:4; Rare:47 | ||||
| chr1:160205210-160205532 | Common:2; Rare:82 | ||||
| chr1:160205741-160205789 | Rare:7 | ||||
| chr1:160261784-160262020 | Rare:52 | ||||
| chr1:160262354-160262769 | Common:2; Rare:112 | ||||
| chr1:160284648-160284698 | Common:1; Rare:10 | ||||
| chr1:160285042-160285229 | Common:3; Rare:75; Clinvar:4; Clinvar (benign):4 | ||||
| chr1:160343166-160343712 | Common:2; Rare:190 | ||||
| chr1:160399977-160400197 | Common:2; Rare:40 | ||||
| chr1:160400328-160400616 | Common:2; Rare:68 |