Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89207231-89207449 | Common:2; Rare:49 | ||||
chr10:89301714-89302047 | Rare:62 | ||||
chr10:89332522-89332533 | Rare:2 | ||||
chr10:89392437-89392658 | Common:7; Rare:56 | ||||
chr10:89414676-89414793 | Common:3; Rare:58 | ||||
chr10:89643914-89644181 | Rare:57 | ||||
chr10:89701446-89701638 | Common:1; Rare:49 | ||||
chr10:90921083-90921277 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
chr10:91162686-91163073 | Common:3; Rare:106 | ||||
chr10:91633047-91633228 | Common:1; Rare:58 | ||||
chr10:91923743-91923821 | Rare:26 | ||||
chr10:92290956-92291390 | Common:5; Rare:134 | ||||
chr10:92573797-92574129 | Common:1; Rare:105 | ||||
chr10:92592960-92593068 | Common:2; Rare:24 | ||||
chr10:92689695-92689955 | Common:1; Rare:87 |