Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101559964-101560226 | Rare:60 | ||||
chr14:101731299-101731435 | Common:3; Rare:35 | ||||
chr14:101948045-101948374 | Common:2; Rare:97 | ||||
chr14:103694218-103694329 | Rare:22 | ||||
chr14:106269126-106269235 | Common:8; Rare:27 | ||||
chr14:106593195-106593296 | Rare:29 | ||||
chr15:22494618-22494902 | Common:1; Rare:35 | ||||
chr15:22665203-22665312 | Rare:19 | ||||
chr15:29730440-29730611 | Rare:38 | ||||
chr15:32536405-32536773 | Common:2; Rare:38 | ||||
chr15:39585473-39585996 | Common:3; Rare:90 | ||||
chr15:45279218-45279417 | Common:1; Rare:78 | ||||
chr15:48515385-48515702 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr15:51094657-51094957 | Common:7; Rare:79 | ||||
chr15:61558942-61559173 | Common:2; Rare:42 |