Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10295476-10295761 | Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
chr1:11643637-11643830 | Common:4; Rare:39 | ||||
chr1:11908223-11908392 | Common:27; Rare:191 | ||||
chr1:15834301-15834550 | Rare:82 | ||||
chr1:15834842-15835133 | Common:2; Rare:130 | ||||
chr1:15835804-15836139 | Common:6; Rare:162 | ||||
chr1:15849361-15849492 | Common:1; Rare:26 | ||||
chr1:15850118-15850289 | Rare:39 | ||||
chr1:15886300-15886583 | Rare:74 | ||||
chr1:16474103-16474321 | Rare:53 | ||||
chr1:16499216-16499378 | Rare:78 | ||||
chr1:16514277-16514710 | Common:5; Rare:138 | ||||
chr1:16644637-16644839 | Common:1; Rare:3 | ||||
chr1:16895579-16895990 | Common:7; Rare:82 | ||||
chr1:16904800-16904974 | Common:2; Rare:23 |