Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50705188-50705489 | Common:1; Rare:70 | ||||
chr22:50798822-50798838 | Rare:7 | ||||
chr3:3038545-3038580 | Common:1; Rare:1 | ||||
chr3:3152564-3152627 | Rare:23 | ||||
chr3:4732880-4733144 | Common:1; Rare:67; Clinvar (benign):1 | ||||
chr3:4811188-4811304 | Rare:24 | ||||
chr3:4831346-4831376 | Rare:6 | ||||
chr3:4836586-4836854 | Common:6; Rare:53 | ||||
chr3:4868567-4868663 | Rare:40 | ||||
chr3:4978322-4978548 | Common:2; Rare:63 | ||||
chr3:9349336-9349585 | Rare:40 | ||||
chr3:9391347-9391526 | Common:2; Rare:29 | ||||
chr3:9396607-9396698 | Rare:41 | ||||
chr3:9977079-9977158 | Rare:16 | ||||
chr3:10088332-10088524 | Rare:53; Clinvar:3 |