EnhancerDB
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Enhancers that regulate FAM96B[ENSG00000166595.7]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr16 66890954 66896750 enh75837 66968326 71576
Muscle (A673) Prostate (RWPE1)
chr16 66899825 66903995 enh16730 66968326 64331
Pancreas Placenta
chr16 66906996 66907469 vista22766 66968326 60857
VISTA
chr16 66928689 66941975 enh16731 66968326 26351
Bone Marrow (K562) Liver (HepG2) Cervix (HeLa-S3) Brain (SK-N-SH) Large Intestine Prostate (RWPE1) Esophagus Astrocyte Ovary Bone (Osteoblast) Lung Stomach Muscle (A673) Placenta Breast Lung (PC-9) Pancreas Muscle (Myotube) Uterus Heart
chr16 66937076 66939560 vista634 66968326 28766
VISTA
chr16 66937613 66937811 vista22767 66968326 30515
VISTA
chr16 66939054 66939376 vista22768 66968326 28950
VISTA
chr16 66939830 66939961 vista22769 66968326 28365
VISTA
chr16 66960903 66961306 vista22770 66968326 7020
VISTA
chr16 66962213 66962449 vista22771 66968326 5877
VISTA
chr16 66978678 66984881 enh89812 66968326 10352
Uterus Prostate (RWPE1)
chr16 66985369 66989735 enh52296 66968326 17043
Esophagus Large Intestine
chr16 66988106 66988414 vista22772 66968326 19780
VISTA
chr16 66993598 66994056 vista22773 66968326 25272
VISTA
chr16 67006845 67015235 enh62558 66968326 38519
Prostate (RWPE1) Esophagus Muscle (A673) Thyroid Uterus Stomach
chr16 67011641 67011860 vista22774 66968326 43315
VISTA
chr16 67018722 67018975 vista22775 66968326 50396
VISTA
chr16 67030331 67030579 vista22776 66968326 62005
VISTA
chr16 67045225 67056815 enh47964 66968326 76899
Bone Marrow (K562) Cervix (HeLa-S3) Prostate (RWPE1) Lung Uterus Neural Stem Cells (H9) Thymus
chr16 67047765 67048035 vista22777 66968326 79439
VISTA
Transcript facotrs that regulate FAM96B[ENSG00000166595.7]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
SNPs associated with FAM96B[ENSG00000166595.7], confirmed by eQTL
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Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr16 67781690 rs142917696 G A 813364 Esophagus 0.0359976 4497707
chr16 66134411 rs185141775 C T 831548 Esophagus 0.119803 4490257
chr16 66894656 rs3026093 T C 71303 Esophagus 4.74597e-13 4494208
chr16 66941016 rs9934391 C T 24943 Heart 0.157197 4494517
chr16 66347295 rs8059293 C T 618664 Pancreas 0.315991 4491785
chr16 66191063 rs72782323 C T 774896 Thyroid 0.204833 4490813
chr16 66097380 rs78788884 G A 868579 Stomach 0.245288 4490082
chr16 66583028 rs3743713 C T 382931 Adrenal 0.343713 4493113
Details of FAM96B[ENSG00000166595.7]
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Genomic Location chr16:66965959-66968326[-]
TSS 66968326
Gene Name FAM96B
Ensembl ID ENSG00000166595.7
ENTREZID 51647
Uniprot
Q9Y3D0
Protein Name
Mitotic spindle-associated MMXD complex subunit MIP18
Expression levels of FAM96B[ENSG00000166595.7]
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