Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36951473-36951549 | Rare:21 | ||||
chr20:36951551-36951579 | Rare:11; Clinvar:1; Clinvar (benign):1 | ||||
chr20:36951589-36951851 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):4 | ||||
chr20:37178865-37179173 | Rare:87 | ||||
chr20:37289534-37289677 | Common:1; Rare:43 | ||||
chr20:37345994-37346150 | Rare:39 | ||||
chr20:37521164-37521265 | Common:1; Rare:29 | ||||
chr20:37527821-37528196 | Common:5; Rare:136 | ||||
chr20:38033404-38033775 | Common:2; Rare:109 | ||||
chr20:38165188-38165469 | Common:1; Rare:97 | ||||
chr20:38166429-38166636 | Common:5; Rare:39 | ||||
chr20:38260118-38260282 | Rare:27 | ||||
chr20:38472642-38472847 | Common:1; Rare:71 | ||||
chr20:38805596-38805750 | Common:2; Rare:35 | ||||
chr20:38926221-38926444 | Common:2; Rare:86 |