Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:65227587-65227877 | Rare:83 | ||||
chr2:66434954-66435171 | Common:1; Rare:49 | ||||
chr2:68157474-68157955 | Common:2; Rare:248 | ||||
chr2:68467292-68467603 | Common:1; Rare:77 | ||||
chr2:69387172-69387406 | Rare:64; Clinvar:2 | ||||
chr2:70087340-70088008 | Common:2; Rare:225 | ||||
chr2:70978571-70978636 | Rare:23 | ||||
chr2:71130220-71130371 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71130537-71130685 | Common:2; Rare:49 | ||||
chr2:74147821-74148124 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
chr2:74421618-74421762 | Rare:47 | ||||
chr2:74458092-74458522 | Common:1; Rare:130 | ||||
chr2:74503337-74503475 | Rare:34 | ||||
chr2:74529648-74530036 | Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74833825-74834148 | Common:1; Rare:97 |