Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:127526425-127526654 | Common:2; Rare:79 | ||||
chr2:127811139-127811216 | Rare:28 | ||||
chr2:127885886-127885991 | Rare:28 | ||||
chr2:128091039-128091354 | Common:8; Rare:102 | ||||
chr2:130181553-130181797 | Common:3; Rare:106 | ||||
chr2:130342118-130342244 | Rare:53; Clinvar:1 | ||||
chr2:130342686-130342927 | Common:3; Rare:78 | ||||
chr2:131093366-131093515 | Common:1; Rare:70 | ||||
chr2:131105194-131105351 | Common:1; Rare:66 | ||||
chr2:131492762-131493092 | Common:8; Rare:99 | ||||
chr2:134918650-134918863 | Common:1; Rare:90 | ||||
chr2:135531172-135531514 | Common:1; Rare:72 | ||||
chr2:137964127-137964586 | Common:2; Rare:82 | ||||
chr2:144517333-144517692 | Common:5; Rare:105; Clinvar:3; Clinvar (benign):4 | ||||
chr2:144518134-144518334 | Common:2; Rare:53 |