Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053360-96053452 | Common:1; Rare:37 | ||||
chr13:99200662-99200898 | Common:6; Rare:108 | ||||
chr13:100088907-100089118 | Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674820-100675140 | Common:4; Rare:132 | ||||
chr13:102596801-102597028 | Common:1; Rare:106 | ||||
chr13:106568091-106568267 | Rare:56 | ||||
chr13:108215502-108215660 | Common:1; Rare:47 | ||||
chr13:108218344-108218499 | Rare:59 | ||||
chr13:110713048-110713261 | Common:2; Rare:86 | ||||
chr13:111153619-111153706 | Common:2; Rare:35 | ||||
chr13:113208641-113208732 | Rare:46 | ||||
chr13:113449140-113449431 | Common:1; Rare:71 | ||||
chr13:113759069-113759278 | Common:1; Rare:57 | ||||
chr13:114281532-114281642 | Common:1; Rare:54 | ||||
chr13:114281844-114282061 | Common:5; Rare:99 |