Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130181571-130181716 | Common:2; Rare:52 | ||||
chr2:130182126-130182339 | Common:2; Rare:85 | ||||
chr2:130342123-130342279 | Rare:64; Clinvar:1 | ||||
chr2:130342681-130342923 | Common:2; Rare:78 | ||||
chr2:131105192-131105351 | Common:1; Rare:67 | ||||
chr2:134918597-134918857 | Common:1; Rare:102 | ||||
chr2:135531178-135531508 | Common:1; Rare:68 | ||||
chr2:135985407-135985642 | Common:4; Rare:109; Clinvar (benign):1 | ||||
chr2:144518377-144518546 | Rare:35 | ||||
chr2:148020681-148021040 | Common:2; Rare:76; Clinvar (benign):2 | ||||
chr2:149587192-149587359 | Common:1; Rare:39 | ||||
chr2:149587706-149587877 | Common:1; Rare:47; Clinvar:1 | ||||
chr2:151828419-151828793 | Common:2; Rare:107 | ||||
chr2:152717829-152717967 | Rare:59 | ||||
chr2:158968497-158968685 | Rare:58 |