Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99200667-99200894 | Common:6; Rare:104 | ||||
chr13:99307350-99307533 | Common:1; Rare:27 | ||||
chr13:100088955-100089128 | Rare:63; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596769-102597028 | Common:1; Rare:117 | ||||
chr13:102846477-102846661 | Common:1; Rare:38 | ||||
chr13:106567680-106567757 | Rare:22 | ||||
chr13:106568098-106568288 | Rare:59 | ||||
chr13:108215495-108215732 | Common:1; Rare:63 | ||||
chr13:108218339-108218516 | Rare:67 | ||||
chr13:110914998-110915214 | Common:3; Rare:91 | ||||
chr13:111153628-111153724 | Common:2; Rare:45 | ||||
chr13:112588130-112588412 | Rare:65 | ||||
chr13:112873318-112873459 | Common:3; Rare:13 | ||||
chr13:113208631-113208751 | Rare:69 | ||||
chr14:20333256-20333411 | Common:1; Rare:32 |