Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:172427743-172427963 | Common:1; Rare:75; Clinvar:2 | ||||
chr2:173965266-173965488 | Common:1; Rare:77 | ||||
chr2:174248461-174248785 | Common:2; Rare:105 | ||||
chr2:174395629-174395772 | Common:1; Rare:48 | ||||
chr2:174486981-174487393 | Common:2; Rare:100 | ||||
chr2:175181654-175181740 | Common:3; Rare:44 | ||||
chr2:176002224-176002414 | Common:3; Rare:83 | ||||
chr2:176129573-176129730 | Rare:92 | ||||
chr2:176188538-176188668 | Common:1; Rare:50 | ||||
chr2:177212416-177212802 | Common:4; Rare:158 | ||||
chr2:177215847-177216125 | Rare:70 | ||||
chr2:177263410-177263684 | Common:1; Rare:63 | ||||
chr2:177264563-177264845 | Common:2; Rare:81 | ||||
chr2:177392659-177393076 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
chr2:177552761-177552855 | Common:1; Rare:32 |