Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:91410255-91410445 | Common:1; Rare:69 | ||||
chr10:91633039-91633232 | Common:1; Rare:63 | ||||
chr10:92592952-92593201 | Common:3; Rare:71 | ||||
chr10:93482260-93482451 | Rare:40 | ||||
chr10:93496396-93496749 | Common:4; Rare:92 | ||||
chr10:93601195-93601402 | Common:3; Rare:43 | ||||
chr10:93702497-93702690 | Common:4; Rare:71 | ||||
chr10:94545714-94545884 | Common:3; Rare:61 | ||||
chr10:95290918-95291186 | Common:2; Rare:113 | ||||
chr10:97426044-97426286 | Common:2; Rare:99 | ||||
chr10:97445959-97446225 | Common:1; Rare:73 | ||||
chr10:98446870-98447053 | Rare:53 | ||||
chr10:99430622-99430936 | Common:3; Rare:70 | ||||
chr10:99659247-99659529 | Common:1; Rare:72 | ||||
chr10:99732056-99732331 | Rare:104; Clinvar:4; Clinvar (benign):1 |