Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:41273996-41274271 | Common:3; Rare:35 | ||||
chr9:41358819-41358916 | Common:1; Rare:31 | ||||
chr9:62801242-62801494 | Common:1; Rare:2 | ||||
chr9:62838339-62838448 | Common:2; Rare:4 | ||||
chr9:62898056-62898372 | Common:3; Rare:23 | ||||
chr9:66269833-66270062 | Common:3; Rare:37 | ||||
chr9:83979604-83979687 | Rare:30 | ||||
chr9:89180335-89180519 | Common:1; Rare:27 | ||||
chr9:99819876-99820197 | Common:2; Rare:92 | ||||
chr9:113012164-113012284 | Rare:23 | ||||
chr9:121499726-121499899 | Rare:49 | ||||
chr9:123998953-123999223 | Common:4; Rare:44 | ||||
chr9:128577202-128577505 | Rare:67; Clinvar:4; Clinvar (benign):8 | ||||
chr9:129320826-129321012 | Rare:28 | ||||
chr9:129413765-129413960 | Common:3; Rare:88 |