Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:62798610-62798854 | Rare:46 | ||||
chr20:62838626-62838710 | Rare:28 | ||||
chr20:63534746-63534954 | Common:4; Rare:73 | ||||
chr20:63535588-63535623 | Common:1; Rare:8 | ||||
chr20:63542062-63542227 | Common:2; Rare:69 | ||||
chr20:63864264-63864354 | Rare:19 | ||||
chr20:63865863-63865919 | Common:1; Rare:15 | ||||
chr20:63945649-63945819 | Rare:66 | ||||
chr21:14273701-14274129 | Common:5; Rare:103 | ||||
chr21:15837550-15837735 | Rare:28 | ||||
chr21:17603956-17604145 | Common:1; Rare:28 | ||||
chr21:25909230-25909432 | Common:3; Rare:49 | ||||
chr21:29002753-29002811 | Common:1; Rare:25 | ||||
chr21:31667086-31667330 | Rare:59; Clinvar:1; Clinvar (pathogenic):7 | ||||
chr21:31685198-31685403 | Common:1; Rare:58 |