Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36797283-36797542 | Rare:56 | ||||
chr19:38004580-38004754 | Common:2; Rare:40 | ||||
chr19:46860837-46861126 | Common:3; Rare:94 | ||||
chr19:48966257-48966681 | Rare:142; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr2:28391245-28391304 | Rare:11 | ||||
chr2:38114101-38114295 | Common:1; Rare:39 | ||||
chr2:55923027-55923158 | Rare:29 | ||||
chr2:100819036-100819215 | Common:1; Rare:28 | ||||
chr2:102020679-102020927 | Rare:64 | ||||
chr2:111495008-111495369 | Common:1; Rare:51 | ||||
chr2:112276132-112276326 | Rare:55 | ||||
chr2:156334489-156334790 | Rare:65 | ||||
chr2:187550909-187551209 | Common:2; Rare:41 | ||||
chr2:227818189-227818373 | Rare:33 | ||||
chr2:227862793-227862947 | Common:1; Rare:23 |