Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:89213905-89214044 | Common:1; Rare:39 | ||||
chr2:89222441-89222649 | Rare:41 | ||||
chr2:89268487-89268610 | Rare:25 | ||||
chr2:89297756-89297884 | Rare:5 | ||||
chr2:89320111-89320237 | Common:3; Rare:35 | ||||
chr2:89585579-89585834 | Rare:1 | ||||
chr2:89913883-89914051 | Common:1; Rare:26 | ||||
chr2:90038774-90038924 | Common:1; Rare:54 | ||||
chr2:90153923-90154078 | Rare:22 | ||||
chr2:90159719-90159843 | Rare:9 | ||||
chr2:91659910-91660045 | Rare:22 | ||||
chr2:95525731-95525973 | Common:1; Rare:40 | ||||
chr2:95526693-95526798 | Common:1; Rare:32 | ||||
chr2:96010464-96010574 | Rare:30 | ||||
chr2:96254058-96254267 | Rare:50; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 |