Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46180861-46181015 | Rare:35 | ||||
chr19:49492296-49492361 | Rare:17 | ||||
chr2:10788697-10788974 | Common:2; Rare:79 | ||||
chr2:47906331-47906580 | Rare:103 | ||||
chr2:74503967-74504229 | Common:2; Rare:52 | ||||
chr2:162071188-162071343 | Rare:32 | ||||
chr2:176637581-176637749 | Common:2; Rare:58 | ||||
chr21:46125607-46125920 | Common:4; Rare:157; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr22:50526981-50527271 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr3:42654389-42654635 | Rare:72 | ||||
chr3:49357222-49357339 | Rare:32 | ||||
chr3:51393036-51393139 | Rare:37 | ||||
chr3:52693719-52694089 | Common:1; Rare:91 | ||||
chr3:75435066-75435339 | Common:3; Rare:100 | ||||
chr3:101676267-101676474 | Common:2; Rare:69 |