Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45851719-45851789 | Rare:11 | ||||
chr13:46052623-46052877 | Common:2; Rare:65 | ||||
chr13:46211748-46212034 | Common:2; Rare:82 | ||||
chr13:46553056-46553193 | Common:2; Rare:47 | ||||
chr13:46797094-46797368 | Common:3; Rare:90 | ||||
chr13:48001265-48001445 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
chr13:48037610-48037789 | Common:1; Rare:81 | ||||
chr13:48037920-48038125 | Common:5; Rare:63 | ||||
chr13:48095062-48095279 | Common:1; Rare:101 | ||||
chr13:48303656-48303900 | Rare:82; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48532643-48532856 | Common:3; Rare:77 | ||||
chr13:48533069-48533315 | Common:1; Rare:70 | ||||
chr13:48975780-48975928 | Common:1; Rare:53 | ||||
chr13:48976144-48976209 | Rare:19 | ||||
chr13:48976366-48976837 | Common:3; Rare:145 |