Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88583309-88583500 | Rare:41 | ||||
chr10:88990559-88990810 | Common:2; Rare:70; Clinvar (benign):2 | ||||
chr10:89247566-89247720 | Common:3; Rare:45; Clinvar:6; Clinvar (benign):2 | ||||
chr10:89251751-89252191 | Common:3; Rare:121; Clinvar:5 | ||||
chr10:89301886-89302050 | Rare:33 | ||||
chr10:89332422-89332527 | Common:3; Rare:18 | ||||
chr10:89414510-89414765 | Common:3; Rare:88 | ||||
chr10:89644970-89645291 | Common:4; Rare:142 | ||||
chr10:89701424-89701617 | Common:1; Rare:51 | ||||
chr10:91798124-91798504 | Common:2; Rare:133 | ||||
chr10:91798725-91798873 | Rare:35 | ||||
chr10:92291042-92291403 | Common:5; Rare:112 | ||||
chr10:92574040-92574183 | Common:1; Rare:47 | ||||
chr10:92592951-92593068 | Common:2; Rare:26 | ||||
chr10:92689704-92689974 | Common:2; Rare:90 |