Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72727600-72727912 | Common:4; Rare:107 | ||||
chr13:72781926-72782194 | Rare:95 | ||||
chr13:100088819-100089117 | Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597024 | Common:1; Rare:109 | ||||
chr13:102798915-102799180 | Common:1; Rare:54 | ||||
chr13:102845679-102845944 | Common:6; Rare:76; Clinvar (benign):3 | ||||
chr13:108218287-108218520 | Common:1; Rare:88 | ||||
chr13:110307060-110307500 | Common:6; Rare:145; Clinvar:1; Clinvar (benign):8 | ||||
chr13:110307592-110307778 | Common:2; Rare:49 | ||||
chr13:113208632-113208752 | Rare:68 | ||||
chr13:113297003-113297298 | Common:1; Rare:118 | ||||
chr13:113490685-113491145 | Common:4; Rare:172 | ||||
chr13:113863934-113864160 | Common:2; Rare:55 | ||||
chr14:20455087-20455281 | Common:2; Rare:63 | ||||
chr14:20461379-20461673 | Common:1; Rare:89 |