Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:165768772-165768929 | Common:1; Rare:69 | ||||
chr1:167935800-167936247 | Common:1; Rare:127 | ||||
chr1:167936553-167936994 | Common:1; Rare:157 | ||||
chr1:168225714-168226062 | Common:4; Rare:111 | ||||
chr1:169367739-169368263 | Common:3; Rare:109 | ||||
chr1:169485932-169486139 | Rare:51; Clinvar:1 | ||||
chr1:170531952-170532135 | Common:2; Rare:50 | ||||
chr1:171485373-171485593 | Rare:84 | ||||
chr1:171841360-171841547 | Common:3; Rare:57 | ||||
chr1:173476965-173477492 | Common:6; Rare:175 | ||||
chr1:173824384-173824708 | Rare:59; Clinvar:1 | ||||
chr1:179081889-179082102 | Common:1; Rare:65 | ||||
chr1:179293682-179293829 | Common:1; Rare:53 | ||||
chr1:179877755-179877884 | Rare:31 | ||||
chr1:179882488-179882870 | Rare:182; Clinvar:8; Clinvar (benign):2 |