Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:75635798-75635874 | Common:1; Rare:19 | ||||
chr13:75636048-75636374 | Common:2; Rare:77 | ||||
chr13:76991932-76992181 | Common:3; Rare:119; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
chr13:78659128-78659226 | Common:2; Rare:73 | ||||
chr13:95301410-95301539 | Rare:35 | ||||
chr13:95676975-95677182 | Common:2; Rare:67 | ||||
chr13:96053358-96053545 | Common:2; Rare:79 | ||||
chr13:99200687-99200909 | Common:6; Rare:106 | ||||
chr13:100088947-100089117 | Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674778-100675055 | Common:3; Rare:112 | ||||
chr13:102596805-102597035 | Common:1; Rare:111 | ||||
chr13:102773719-102773860 | Rare:60 | ||||
chr13:102845735-102846089 | Common:8; Rare:92; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106568085-106568267 | Rare:58 | ||||
chr13:108215495-108215649 | Common:1; Rare:45 |