Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:53228130-53228279 | Rare:51 | ||||
chr3:57583946-57584146 | Rare:41 | ||||
chr3:63912505-63912680 | Common:2; Rare:67 | ||||
chr3:69937683-69937760 | Rare:16 | ||||
chr3:75435021-75435377 | Common:4; Rare:124 | ||||
chr3:81761530-81761605 | Common:5; Rare:24; Clinvar (benign):1 | ||||
chr3:101676284-101676481 | Rare:62 | ||||
chr3:107240600-107240739 | Rare:60 | ||||
chr3:153163270-153163620 | Common:1; Rare:86 | ||||
chr3:153164023-153164269 | Common:3; Rare:53 | ||||
chr3:160515233-160515496 | Common:1; Rare:49 | ||||
chr3:184323498-184323813 | Common:3; Rare:78 | ||||
chr3:184323934-184324233 | Common:2; Rare:72 | ||||
chr3:184710792-184710901 | Rare:27 | ||||
chr3:197627846-197628086 | Common:8; Rare:93 |