Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39562072-39562361 | Rare:63 | ||||
chr1:39569571-39569999 | Common:1; Rare:126 | ||||
chr1:39572121-39572532 | Common:2; Rare:78 | ||||
chr1:39738748-39738926 | Common:2; Rare:45 | ||||
chr1:39882835-39883166 | Common:3; Rare:60 | ||||
chr1:39883345-39883379 | Rare:9 | ||||
chr1:39883441-39883543 | Common:1; Rare:46; Clinvar (pathogenic):1 | ||||
chr1:40040115-40040256 | Common:2; Rare:24 | ||||
chr1:40040438-40040814 | Common:3; Rare:116 | ||||
chr1:40161254-40161444 | Rare:60 | ||||
chr1:40257897-40258373 | Common:4; Rare:139; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40374465-40374678 | Common:12; Rare:43 | ||||
chr1:40449958-40450227 | Common:5; Rare:96 | ||||
chr1:40508666-40508816 | Common:4; Rare:42 | ||||
chr1:40531487-40531700 | Rare:59 |