Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30617754-30618000 | Common:1; Rare:82 | ||||
chr13:30735407-30735602 | Common:2; Rare:45 | ||||
chr13:32315445-32315539 | Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chr13:32586248-32586582 | Common:2; Rare:101 | ||||
chr13:33285703-33285880 | Rare:39 | ||||
chr13:33818015-33818197 | Common:1; Rare:79 | ||||
chr13:35476655-35476749 | Common:1; Rare:12 | ||||
chr13:36131167-36131480 | Common:1; Rare:77 | ||||
chr13:36297794-36297909 | Rare:42 | ||||
chr13:36346301-36346460 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36999288-36999465 | Rare:69 | ||||
chr13:37059600-37059737 | Common:1; Rare:47 | ||||
chr13:37598556-37598903 | Common:2; Rare:103 | ||||
chr13:38350254-38350410 | Rare:45 | ||||
chr13:39038087-39038381 | Common:1; Rare:72 |