Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235161109-235161429 | Common:1; Rare:183 | ||||
chr1:235326773-235327020 | Common:2; Rare:62 | ||||
chr1:235327117-235327318 | Rare:54 | ||||
chr1:235327889-235327939 | Rare:15 | ||||
chr1:235328043-235328220 | Common:1; Rare:57 | ||||
chr1:235328525-235328656 | Common:2; Rare:46 | ||||
chr1:235328734-235329076 | Common:1; Rare:109 | ||||
chr1:235329257-235329395 | Rare:33 | ||||
chr1:235367229-235367525 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
chr1:235503800-235504203 | Common:8; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
chr1:235504284-235505277 | Common:7; Rare:261 | ||||
chr1:235866806-235867291 | Common:4; Rare:147 | ||||
chr1:235883661-235883839 | Rare:33 | ||||
chr1:236064679-236064904 | Common:1; Rare:79 | ||||
chr1:236065059-236065370 | Common:3; Rare:117; Clinvar (pathogenic):1 |