Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45986983-45987175 | Common:2; Rare:70; Clinvar:12; Clinvar (benign):5 | ||||
chr21:46097274-46097630 | Common:3; Rare:75 | ||||
chr21:46098020-46098172 | Rare:53; Clinvar (benign):1 | ||||
chr21:46286233-46286406 | Common:4; Rare:66 | ||||
chr22:17159251-17159385 | Common:4; Rare:69 | ||||
chr22:17628615-17628872 | Common:2; Rare:86 | ||||
chr22:18024520-18024599 | Rare:21 | ||||
chr22:19432325-19432606 | Common:3; Rare:120 | ||||
chr22:19447690-19447738 | Rare:26 | ||||
chr22:19941725-19942126 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
chr22:20117200-20117561 | Common:3; Rare:111 | ||||
chr22:20495781-20495994 | Common:2; Rare:81 | ||||
chr22:20858780-20859093 | Common:4; Rare:155; Clinvar:3; Clinvar (benign):3 | ||||
chr22:23751110-23751209 | Common:1; Rare:32 | ||||
chr22:23857809-23857920 | Common:2; Rare:39 |