Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190880616-190880890 | Common:4; Rare:92 | ||||
chr2:191014115-191014423 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191245231-191245541 | Common:3; Rare:98 | ||||
chr2:191677831-191678177 | Common:4; Rare:100 | ||||
chr2:196068782-196068921 | Common:1; Rare:41 | ||||
chr2:197434972-197435164 | Rare:68 | ||||
chr2:197453233-197453556 | Rare:108 | ||||
chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515835-197516098 | Common:2; Rare:96 | ||||
chr2:200510040-200510113 | Rare:25 | ||||
chr2:200609105-200609353 | Rare:63 | ||||
chr2:200811385-200811589 | Common:1; Rare:71 | ||||
chr2:200888994-200889461 | Common:3; Rare:149 | ||||
chr2:201071604-201072047 | Rare:95 | ||||
chr2:201451435-201451816 | Common:2; Rare:97 |