Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015764-213015927 | Rare:49 | ||||
chr1:217078203-217078341 | Rare:21 | ||||
chr1:217631020-217631379 | Common:2; Rare:100 | ||||
chr1:218345764-218346096 | Common:5; Rare:103; Clinvar:9; Clinvar (benign):4 | ||||
chr1:218346145-218346306 | Rare:25 | ||||
chr1:219173766-219173902 | Common:1; Rare:73 | ||||
chr1:220272382-220272618 | Rare:70; Clinvar:5 | ||||
chr1:222589851-222589947 | Common:2; Rare:28 | ||||
chr1:222712443-222712875 | Common:3; Rare:152 | ||||
chr1:224183089-224183289 | Common:3; Rare:94 | ||||
chr1:224330128-224330439 | Common:6; Rare:94 | ||||
chr1:225428010-225428270 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):2 | ||||
chr1:225777723-225777910 | Common:3; Rare:58 | ||||
chr1:225924248-225924440 | Common:5; Rare:47 | ||||
chr1:225999310-225999616 | Common:2; Rare:104 |