Enhancers that regulate CHTF8[ENSG00000168802.8]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr16 69061972 69067955 enh52302 69166487 98532
chr16 69068389 69073535 enh62562 69166487 92952
chr16 69081060 69101258 enh31894 69166487 65229
chr16 69101372 69114315 enh16749 69166487 52172
chr16 69106233 69106613 vista22841 69166487 59874
chr16 69120974 69133979 enh62563 69166487 32508
chr16 69121214 69121414 vista22842 69166487 45073
chr16 69203285 69215888 enh31895 69166487 36798
chr16 69218925 69230135 enh4111 69166487 52438
chr16 69225511 69225823 vista22843 69166487 59024
chr16 69230445 69240855 enh57691 69166487 63958
chr16 69249331 69261375 enh31896 69166487 82844

Transcript facotrs that regulate CHTF8[ENSG00000168802.8]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr16 69461985 rs8063454 C G 295498 Esophagus 0.171781 4505775
chr16 69123280 rs77073902 A C 28633 Spleen 0.34785 4504258
chr16 68742448 rs142691602 T C 409465 Ovary 0.161554 4502028
chr16 69432924 rs145890132 C T 266437 Thyroid 0.157203 4505501
chr16 69164212 rs370308709 TTTTG T 0 Liver 0.358 4504406
chr16 69958407 rs766182398 AC A 791920 Adrenal 0.416329 4509028

Genomic Location chr16:69151913-69166487[-]
TSS 69166487
Gene Name CHTF8
Ensembl ID ENSG00000168802.8
ENTREZID 54921
Uniprot
P0CG12
L0R4W3
P0CG13
Protein Name
Alternative protein CHTF8
Chromosome transmission fidelity protein 8 homolog
Chromosome transmission fidelity protein 8 homolog isoform 2