Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100266696-100267030 | Common:5; Rare:60 | ||||
chr1:100351573-100351772 | Common:3; Rare:104 | ||||
chr1:100352156-100353019 | Common:9; Rare:495; Clinvar (benign):4 | ||||
chr1:100894634-100895074 | Common:3; Rare:180 | ||||
chr1:100895660-100896235 | Common:1; Rare:288 | ||||
chr1:100896615-100896793 | Rare:49 | ||||
chr1:101025713-101025973 | Common:3; Rare:178 | ||||
chr1:103525441-103525759 | Rare:92 | ||||
chr1:103525845-103526073 | Common:1; Rare:133 | ||||
chr1:107056498-107056887 | Common:4; Rare:391 | ||||
chr1:107056818-107057327 | Common:1; Rare:303 | ||||
chr1:107141040-107141460 | Common:2; Rare:153 | ||||
chr1:107688389-107688676 | Rare:147 | ||||
chr1:107963680-107964083 | Common:2; Rare:103 | ||||
chr1:107964447-107964847 | Common:7; Rare:254 |