Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:49463146-49463407 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52420101-52420364 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52576928-52577284 | Common:6; Rare:128 | ||||
chr6:52671031-52671167 | Rare:39 | ||||
chr6:52995267-52995808 | Common:4; Rare:227 | ||||
chr6:53065574-53065604 | Rare:9 | ||||
chr6:53348867-53349222 | Common:2; Rare:141 | ||||
chr6:57089872-57090219 | Rare:129 | ||||
chr6:57172524-57172550 | Rare:6 | ||||
chr6:57172556-57172766 | Common:1; Rare:69 | ||||
chr6:57222272-57222411 | Rare:53 | ||||
chr6:69796872-69797236 | Common:2; Rare:104; Clinvar:6; Clinvar (benign):2 | ||||
chr6:70413184-70413437 | Common:1; Rare:70 | ||||
chr6:73263163-73263248 | Common:2; Rare:17 | ||||
chr6:73518352-73519230 | Common:1; Rare:262 |