Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:85595555-85595770 | Common:2; Rare:69 | ||||
chr2:85612030-85612103 | Rare:19 | ||||
chr2:85616024-85616245 | Common:1; Rare:85 | ||||
chr2:86105849-86106257 | Common:3; Rare:112 | ||||
chr2:86195391-86195535 | Common:4; Rare:52 | ||||
chr2:95165647-95165817 | Rare:52 | ||||
chr2:96208264-96208403 | Rare:71 | ||||
chr2:96208816-96208849 | Rare:16 | ||||
chr2:96265978-96266348 | Common:2; Rare:112 | ||||
chr2:96305475-96305690 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
chr2:96335592-96335812 | Common:1; Rare:72 | ||||
chr2:98608426-98608659 | Common:1; Rare:104; Clinvar (benign):1 | ||||
chr2:99180977-99181234 | Common:2; Rare:73 | ||||
chr2:100562715-100563050 | Common:3; Rare:106 | ||||
chr2:101002162-101002318 | Rare:61 |