Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189783965-189784064 | Common:2; Rare:31 | ||||
chr2:189784275-189784547 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190319729-190319973 | Common:5; Rare:91; Clinvar (benign):5 | ||||
chr2:190880623-190880859 | Common:4; Rare:80 | ||||
chr2:191246152-191246200 | Rare:16 | ||||
chr2:191677856-191678161 | Common:4; Rare:86 | ||||
chr2:191678803-191679040 | Common:1; Rare:69 | ||||
chr2:195657119-195657320 | Common:1; Rare:61 | ||||
chr2:196068801-196068899 | Common:1; Rare:23 | ||||
chr2:197434980-197435186 | Rare:69 | ||||
chr2:197453249-197453557 | Rare:104 | ||||
chr2:197499788-197500131 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
chr2:197500198-197500446 | Common:1; Rare:106 | ||||
chr2:197515841-197516098 | Common:1; Rare:94 | ||||
chr2:199911144-199911354 | Rare:62 |