Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:33142414-33142635 | Common:6; Rare:46 | ||||
chr6:33142693-33142944 | Common:12; Rare:42 | ||||
chr6:33193517-33193612 | Common:3; Rare:23 | ||||
chr6:33249238-33249587 | Rare:103 | ||||
chr6:33418942-33419236 | Common:1; Rare:49 | ||||
chr6:33425711-33425897 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr6:33443623-33444240 | Common:3; Rare:142; Clinvar:3; Clinvar (benign):11 | ||||
chr6:33633582-33633910 | Common:6; Rare:93 | ||||
chr6:33694753-33694993 | Common:1; Rare:69 | ||||
chr6:33787939-33788127 | Common:3; Rare:37 | ||||
chr6:34240754-34241127 | Common:3; Rare:112 | ||||
chr6:34526972-34527408 | Common:5; Rare:101 | ||||
chr6:35052279-35052539 | Common:1; Rare:50 | ||||
chr6:35318455-35318657 | Common:2; Rare:39 | ||||
chr6:35486726-35486879 | Common:1; Rare:27 |