Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:31255064-31255402 | Common:3; Rare:69 | ||||
chr21:38807170-38807391 | Rare:34 | ||||
chr21:41951140-41951459 | Common:1; Rare:66 | ||||
chr21:43370343-43370496 | Common:1; Rare:30 | ||||
chr22:19688027-19688173 | Rare:34 | ||||
chr22:22298052-22298175 | Common:1; Rare:43 | ||||
chr22:28796125-28796350 | Rare:52 | ||||
chr22:30969044-30969283 | Common:2; Rare:67 | ||||
chr22:31278103-31278357 | Common:2; Rare:55 | ||||
chr22:36288778-36289152 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):5 | ||||
chr22:37805943-37806136 | Rare:61 | ||||
chr22:37806166-37806434 | Common:3; Rare:55 | ||||
chr22:38336134-38336337 | Rare:58 | ||||
chr22:41197497-41197696 | Common:2; Rare:57 | ||||
chr22:41529276-41529489 | Rare:54 |