Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:36060499-36060613 | Common:3; Rare:39 | ||||
chr21:36990212-36990258 | Common:3; Rare:17; Clinvar (benign):3 | ||||
chr21:37073015-37073350 | Common:5; Rare:133 | ||||
chr21:37267518-37267699 | Common:2; Rare:69 | ||||
chr21:39183390-39183581 | Common:5; Rare:78 | ||||
chr21:39445768-39445875 | Common:2; Rare:33 | ||||
chr21:41508066-41508335 | Common:2; Rare:61 | ||||
chr21:41767007-41767173 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
chr21:42514441-42514551 | Rare:23 | ||||
chr21:42893073-42893336 | Common:3; Rare:87 | ||||
chr21:44299984-44300100 | Rare:46 | ||||
chr21:44801774-44801880 | Rare:43 | ||||
chr21:44873626-44874040 | Common:8; Rare:166 | ||||
chr21:45287879-45288085 | Common:5; Rare:80 | ||||
chr21:45981519-45981827 | Common:23; Rare:71; Clinvar (benign):2 |