Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1231923-1232262 | Rare:118; Clinvar (benign):2 | ||||
chr1:1273768-1274026 | Common:1; Rare:104 | ||||
chr1:1324600-1324827 | Common:3; Rare:127 | ||||
chr1:1358497-1358769 | Common:1; Rare:100 | ||||
chr1:1399290-1399620 | Common:1; Rare:149 | ||||
chr1:1407190-1407387 | Common:1; Rare:90 | ||||
chr1:1435606-1435714 | Rare:37 | ||||
chr1:1574541-1574963 | Common:1; Rare:197 | ||||
chr1:1632044-1632198 | Common:2; Rare:51 | ||||
chr1:1658897-1659051 | Common:2; Rare:65 | ||||
chr1:1724267-1724561 | Common:5; Rare:111 | ||||
chr1:2391543-2391948 | Common:2; Rare:142 | ||||
chr1:2586282-2586497 | Common:1; Rare:72 | ||||
chr1:3624748-3625087 | Common:1; Rare:108 | ||||
chr1:3772434-3772779 | Common:3; Rare:84 |