Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:46030551-46030731 | Common:1; Rare:62 | ||||
chr10:46398258-46398437 | Common:4; Rare:73 | ||||
chr10:46911366-46911481 | Rare:9 | ||||
chr10:48605036-48605225 | Common:1; Rare:55 | ||||
chr10:49077217-49077529 | Rare:81 | ||||
chr10:49115437-49115802 | Common:1; Rare:97 | ||||
chr10:49941891-49942118 | Rare:71 | ||||
chr10:50067837-50068004 | Common:4; Rare:79 | ||||
chr10:50623876-50624079 | Common:1; Rare:80 | ||||
chr10:50624919-50625010 | Common:1; Rare:32 | ||||
chr10:50625156-50625207 | Rare:16 | ||||
chr10:50739916-50739982 | Rare:13 | ||||
chr10:50990628-50991114 | Common:6; Rare:79 | ||||
chr10:51074024-51074322 | Common:5; Rare:75 | ||||
chr10:51074364-51074810 | Common:1; Rare:113; Clinvar (benign):11 |