Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24076230-24076578 | Rare:94 | ||||
chr2:24123272-24123478 | Common:1; Rare:51 | ||||
chr2:25878455-25878742 | Common:3; Rare:88 | ||||
chr2:26033778-26034200 | Common:3; Rare:153 | ||||
chr2:26244602-26244965 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:26345798-26346160 | Common:1; Rare:109 | ||||
chr2:26764215-26764312 | Rare:35 | ||||
chr2:27032824-27032995 | Rare:67 | ||||
chr2:27071604-27071872 | Common:1; Rare:83 | ||||
chr2:27211895-27212041 | Common:3; Rare:53 | ||||
chr2:27212262-27212379 | Common:1; Rare:59 | ||||
chr2:27323063-27323154 | Rare:21 | ||||
chr2:27356750-27356770 | Rare:5 | ||||
chr2:27356774-27357077 | Rare:89 | ||||
chr2:27370310-27370641 | Common:1; Rare:131 |