Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155990028-155990214 | Rare:35 | ||||
chr1:156012503-156012689 | Rare:39 | ||||
chr1:156020853-156021084 | Rare:73 | ||||
chr1:156053806-156053954 | Rare:30 | ||||
chr1:156053956-156054340 | Common:1; Rare:86 | ||||
chr1:156054537-156054910 | Common:4; Rare:99 | ||||
chr1:156054981-156055162 | Common:1; Rare:37 | ||||
chr1:156082463-156082585 | Rare:31 | ||||
chr1:156106421-156106763 | Common:3; Rare:65 | ||||
chr1:156114527-156114845 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
chr1:156123339-156123729 | Common:2; Rare:70 | ||||
chr1:156146975-156147128 | Common:2; Rare:35 | ||||
chr1:156149334-156149690 | Common:1; Rare:77 | ||||
chr1:156150643-156150872 | Common:1; Rare:43 | ||||
chr1:156154321-156154606 | Rare:68 |