Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:41241747-41241966 | Common:1; Rare:56 | ||||
chr1:41241984-41242177 | Common:1; Rare:53 | ||||
chr1:41242288-41242449 | Common:1; Rare:43 | ||||
chr1:41361380-41361479 | Rare:29 | ||||
chr1:41484654-41484881 | Common:3; Rare:55 | ||||
chr1:42035952-42036159 | Common:1; Rare:49 | ||||
chr1:42334410-42334543 | Rare:47 | ||||
chr1:42334754-42334845 | Rare:35 | ||||
chr1:42335095-42335680 | Common:8; Rare:218 | ||||
chr1:42335758-42335929 | Common:3; Rare:32 | ||||
chr1:42456013-42456127 | Rare:36 | ||||
chr1:42456206-42456796 | Common:3; Rare:194 | ||||
chr1:42456851-42457015 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:42462996-42463341 | Common:4; Rare:110 | ||||
chr1:42464055-42464365 | Common:1; Rare:49 |