Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40834583-40834689 | Common:1; Rare:34 | ||||
chr17:41026191-41026276 | Rare:18 | ||||
chr17:41059343-41059414 | Common:1; Rare:14 | ||||
chr17:41110455-41110612 | Rare:30 | ||||
chr17:41114555-41115027 | Common:7; Rare:136 | ||||
chr17:41825755-41826020 | Common:3; Rare:42 | ||||
chr17:41868562-41869067 | Common:7; Rare:109 | ||||
chr17:41871793-41872177 | Rare:90 | ||||
chr17:41894606-41894704 | Rare:23 | ||||
chr17:41894709-41894890 | Common:1; Rare:21 | ||||
chr17:41968994-41969112 | Rare:21 | ||||
chr17:42275540-42275835 | Rare:56 | ||||
chr17:42422624-42422766 | Rare:60; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42697019-42697276 | Common:1; Rare:58 | ||||
chr17:42774426-42774698 | Common:3; Rare:47 |