Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:68515380-68515614 | Common:2; Rare:40 | ||||
chr9:70413065-70413133 | Rare:11 | ||||
chr9:70413394-70413700 | Rare:96 | ||||
chr9:70413884-70414061 | Rare:34 | ||||
chr9:70479946-70480222 | Rare:47 | ||||
chr9:83219210-83219357 | Common:2; Rare:38 | ||||
chr9:91852904-91853067 | Common:2; Rare:41 | ||||
chr9:113462780-113463100 | Rare:50 | ||||
chr9:121499688-121499799 | Rare:36 | ||||
chr9:123097526-123097804 | Rare:45 | ||||
chr9:124658403-124658436 | Rare:6 | ||||
chr9:127184226-127184477 | Common:3; Rare:53 | ||||
chr9:127819621-127819738 | Rare:37; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr9:129320899-129321013 | Rare:15 | ||||
chr9:129698451-129698760 | Common:2; Rare:51 |