Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185301126-185301426 | Common:1; Rare:67 | ||||
chr1:185307049-185307209 | Rare:34 | ||||
chr1:185316952-185317093 | Common:1; Rare:34 | ||||
chr1:185317186-185317469 | Common:1; Rare:82 | ||||
chr1:186375088-186375944 | Common:1; Rare:237 | ||||
chr1:186680333-186680735 | Common:3; Rare:91 | ||||
chr1:192158248-192158583 | Common:1; Rare:59 | ||||
chr1:192159082-192159311 | Rare:65 | ||||
chr1:192808794-192809138 | Common:4; Rare:151 | ||||
chr1:193059280-193059697 | Rare:200 | ||||
chr1:193105384-193105529 | Common:2; Rare:60 | ||||
chr1:193121671-193122216 | Common:3; Rare:191; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193122348-193122470 | Rare:46 | ||||
chr1:193186611-193186654 | Rare:9 | ||||
chr1:197146601-197146808 | Rare:48; Clinvar:3 |