Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:29654826-29654990 | Rare:45 | ||||
chr21:31160680-31160693 | Rare:1 | ||||
chr21:32580172-32580231 | Rare:13 | ||||
chr21:37074428-37074519 | Rare:23 | ||||
chr21:37221323-37221448 | Rare:52 | ||||
chr21:40662977-40663225 | Common:5; Rare:72 | ||||
chr21:42524853-42524989 | Rare:31 | ||||
chr21:42743334-42743575 | Common:2; Rare:46 | ||||
chr21:44304075-44304373 | Common:5; Rare:84 | ||||
chr22:17037150-17037291 | Common:1; Rare:31 | ||||
chr22:17258262-17258555 | Common:3; Rare:50 | ||||
chr22:18970227-18970564 | Common:8; Rare:102 | ||||
chr22:18994021-18994299 | Common:2; Rare:56 | ||||
chr22:19176473-19176586 | Rare:54; Clinvar (pathogenic):1 | ||||
chr22:20702196-20702385 | Common:1; Rare:30 |