Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:138773333-138773547 | Common:2; Rare:95 | ||||
chr6:138773657-138773828 | Common:3; Rare:83 | ||||
chr6:139028442-139028530 | Common:1; Rare:17 | ||||
chr6:139028553-139028875 | Common:1; Rare:66 | ||||
chr6:142147120-142147300 | Common:3; Rare:69 | ||||
chr6:142301848-142302126 | Common:6; Rare:78 | ||||
chr6:143060391-143060494 | Rare:23 | ||||
chr6:143060704-143060935 | Common:7; Rare:81 | ||||
chr6:143450660-143450929 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
chr6:143511638-143512024 | Common:5; Rare:82 | ||||
chr6:143843179-143843425 | Common:2; Rare:78 | ||||
chr6:145814723-145814921 | Common:1; Rare:93 | ||||
chr6:145964306-145964549 | Rare:79 | ||||
chr6:149545989-149546139 | Rare:63 | ||||
chr6:149746473-149746615 | Common:2; Rare:70 |