Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:136028147-136028305 | Common:1; Rare:24 | ||||
chr5:136036349-136036663 | Common:1; Rare:51 | ||||
chr5:136043999-136044123 | Rare:25; Clinvar:1 | ||||
chr5:137752750-137752962 | Rare:47 | ||||
chr5:137752982-137753040 | Rare:18 | ||||
chr5:138019101-138019299 | Common:1; Rare:44 | ||||
chr5:138182459-138182603 | Rare:39 | ||||
chr5:138183575-138183755 | Rare:52 | ||||
chr5:138403748-138403811 | Rare:9 | ||||
chr5:138556102-138556141 | Rare:4 | ||||
chr5:138943070-138943387 | Common:1; Rare:51 | ||||
chr5:139277260-139277431 | Common:2; Rare:34 | ||||
chr5:139325412-139325838 | Rare:126; Clinvar:6; Clinvar (benign):3 | ||||
chr5:139614730-139614965 | Rare:34 | ||||
chr5:140115499-140115765 | Common:1; Rare:50 |