Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28736584-28737045 | Common:3; Rare:143 | ||||
chr1:28737716-28737769 | Rare:19 | ||||
chr1:31065630-31065986 | Common:2; Rare:127 | ||||
chr1:31296726-31297090 | Common:5; Rare:122 | ||||
chr1:31576397-31576566 | Common:1; Rare:65 | ||||
chr1:31576996-31577194 | Rare:40 | ||||
chr1:31644852-31645017 | Common:3; Rare:52 | ||||
chr1:32108467-32108623 | Common:1; Rare:34 | ||||
chr1:32179621-32179776 | Rare:33 | ||||
chr1:32291824-32292178 | Common:1; Rare:100 | ||||
chr1:32394403-32394582 | Common:1; Rare:48 | ||||
chr1:32650933-32651316 | Common:2; Rare:146 | ||||
chr1:32669416-32669539 | Rare:30 | ||||
chr1:32817233-32817689 | Common:1; Rare:122; Clinvar:5; Clinvar (benign):2 | ||||
chr1:33021369-33021701 | Rare:82; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |