Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45474500-45474890 | Common:7; Rare:77 | ||||
chr21:45476350-45476620 | Common:6; Rare:114; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr21:45525253-45525653 | Common:10; Rare:176 | ||||
chr21:45554936-45555690 | Common:78; Rare:471 | ||||
chr21:46295469-46295580 | Common:1; Rare:30 | ||||
chr22:12602016-12602364 | Rare:32 | ||||
chr22:17639527-17639775 | Common:6; Rare:128 | ||||
chr22:17777128-17777354 | Rare:69 | ||||
chr22:17781273-17781443 | Common:3; Rare:27 | ||||
chr22:17972710-17973060 | Common:4; Rare:92 | ||||
chr22:18148413-18148681 | Common:3; Rare:87 | ||||
chr22:19171568-19171739 | Rare:127 | ||||
chr22:19959660-19960110 | Common:14; Rare:117 | ||||
chr22:20212099-20212237 | Rare:36 | ||||
chr22:20564530-20564860 | Rare:89 |