Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214448937-214448991 | Common:1; Rare:11 | ||||
chr1:214451632-214451882 | Common:1; Rare:49 | ||||
chr1:214517492-214517772 | Common:2; Rare:47 | ||||
chr1:214549937-214550107 | Common:2; Rare:24 | ||||
chr1:214614796-214614878 | Rare:21; Clinvar (pathogenic):1 | ||||
chr1:215586218-215586380 | Rare:28 | ||||
chr1:218312635-218313045 | Common:4; Rare:64 | ||||
chr1:218347954-218348375 | Common:4; Rare:98 | ||||
chr1:218348611-218349050 | Common:1; Rare:74 | ||||
chr1:218349293-218349502 | Common:1; Rare:39 | ||||
chr1:218350150-218350389 | Common:3; Rare:48 | ||||
chr1:218368463-218368547 | Rare:15 | ||||
chr1:218368556-218368612 | Rare:9 | ||||
chr1:218372027-218372153 | Rare:30 | ||||
chr1:218374939-218375020 | Rare:10 |