Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29745147-29745316 | Rare:19 | ||||
chr16:30634271-30634561 | Common:1; Rare:72 | ||||
chr16:30659111-30659352 | Rare:85 | ||||
chr16:30875331-30875490 | Rare:52 | ||||
chr16:31191008-31191348 | Common:1; Rare:112; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr16:56917115-56917299 | Rare:31 | ||||
chr16:56991123-56991362 | Common:2; Rare:40 | ||||
chr16:57568609-57568705 | Rare:19 | ||||
chr16:57569176-57569486 | Common:3; Rare:44 | ||||
chr16:67530319-67530699 | Common:1; Rare:67 | ||||
chr16:68183174-68183238 | Rare:14 | ||||
chr16:69563978-69564199 | Common:1; Rare:50 | ||||
chr16:72664968-72665133 | Rare:48 | ||||
chr16:81831816-81831993 | Rare:57 | ||||
chr16:83806177-83806395 | Common:1; Rare:39 |