Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:108601362-108601483 | Common:1; Rare:25 | ||||
chr2:113583981-113584112 | Rare:29 | ||||
chr2:131682380-131682542 | Common:3; Rare:50 | ||||
chr2:132347186-132347494 | Common:3; Rare:68 | ||||
chr2:156334475-156334790 | Rare:69 | ||||
chr2:156341694-156341810 | Rare:38 | ||||
chr2:168211242-168211474 | Common:2; Rare:42 | ||||
chr2:170770772-170771059 | Common:1; Rare:48 | ||||
chr2:176637589-176637753 | Common:3; Rare:59 | ||||
chr2:177117510-177117541 | Rare:7 | ||||
chr2:188994758-188995098 | Rare:71; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr2:212537579-212537905 | Common:2; Rare:73 | ||||
chr2:217928412-217928547 | Common:1; Rare:16 | ||||
chr2:218277071-218277261 | Common:1; Rare:42 | ||||
chr2:219685030-219685319 | Common:1; Rare:79 |