Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:171522291-171522562 | Common:3; Rare:66 | ||||
chr2:171687697-171688026 | Common:1; Rare:89 | ||||
chr2:171922288-171922499 | Rare:81 | ||||
chr2:171999818-171999972 | Common:1; Rare:64 | ||||
chr2:173354612-173354908 | Common:1; Rare:89 | ||||
chr2:174248456-174248744 | Common:1; Rare:87 | ||||
chr2:174395618-174395795 | Common:2; Rare:57 | ||||
chr2:174487037-174487343 | Common:2; Rare:72 | ||||
chr2:176002229-176002398 | Common:2; Rare:69 | ||||
chr2:177212416-177212802 | Common:4; Rare:158 | ||||
chr2:177263419-177263715 | Common:1; Rare:73 | ||||
chr2:177264642-177264898 | Common:2; Rare:79 | ||||
chr2:177392659-177393070 | Common:3; Rare:143; Clinvar:6; Clinvar (benign):4 | ||||
chr2:177552750-177552818 | Rare:29 | ||||
chr2:177618706-177619051 | Common:7; Rare:99 |