| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160262300-160262683 | Common:2; Rare:182 | ||||
| chr1:160343159-160343482 | Rare:254 | ||||
| chr1:161021091-161021491 | Common:3; Rare:145 | ||||
| chr1:161045148-161045316 | Common:1; Rare:29 | ||||
| chr1:161045875-161046077 | Common:2; Rare:103 | ||||
| chr1:161098170-161098430 | Common:2; Rare:64 | ||||
| chr1:161117650-161117860 | Common:2; Rare:92 | ||||
| chr1:161117956-161118183 | Rare:202 | ||||
| chr1:161118150-161118490 | Common:1; Rare:159 | ||||
| chr1:161132502-161132697 | Common:2; Rare:103 | ||||
| chr1:161132775-161133234 | Common:3; Rare:157 | ||||
| chr1:161153460-161153800 | Rare:58 | ||||
| chr1:161154070-161154430 | Common:2; Rare:123 | ||||
| chr1:161159389-161159619 | Common:2; Rare:109 | ||||
| chr1:161166249-161166646 | Common:8; Rare:181; Clinvar:10; Clinvar (benign):4 |