EnhancerDB
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Enhancers that regulate NGB[ENSG00000165553.4]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr14 77639599 77639692 vista18567 77737655 97963
VISTA
chr14 77640033 77640278 vista18568 77737655 97377
VISTA
chr14 77648205 77655755 enh3339 77737655 81900
Large Intestine Prostate (RWPE1) Esophagus Astrocyte Ovary Colon (HCT116) Thyroid Blood (Karpas-422) Pancreas
chr14 77668425 77672975 enh96538 77737655 64680
Epithelial (MCF-7)
chr14 77764185 77772275 enh51885 77737655 26530
Liver (HepG2) Large Intestine Stomach
chr14 77773605 77785675 enh15799 77737655 35950
Prostate (PC-3) Liver (HepG2) Cervix (HeLa-S3) Brain (SK-N-SH) Large Intestine Prostate (RWPE1) Esophagus Bone (Osteoblast) Muscle (A673) Placenta Thyroid Uterus Neural Stem Cells (H9) Thymus Stomach
chr14 77780620 77780713 vista18569 77737655 42965
VISTA
chr14 77818165 77822315 enh92558 77737655 80510
Liver (HepG2)
chr14 77822525 77841023 enh3340 77737655 84870
Blood (OCI-LY7) Blood (GM12878) Blood (Karpas-422) Blood (T-cell) Stomach
chr14 77826239 77826291 vista18570 77737655 88584
VISTA
Transcript facotrs that regulate NGB[ENSG00000165553.4]
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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 NGB[ENSG00000165553.4], 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
chr14 77509229 rs61991646 C T 222597 Pancreas 0.028704 3676675
chr14 77455035 rs2885800 G A 276791 Stomach 0.177736 3675989
Details of NGB[ENSG00000165553.4]
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Genomic Location chr14:77731826-77737655[-]
TSS 77737655
Gene Name NGB
Ensembl ID ENSG00000165553.4
ENTREZID 58157
Uniprot
Q9NPG2
A0M8W9
Protein Name
Globin H
Neuroglobin
Expression levels of NGB[ENSG00000165553.4]
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