Enhancers that regulate NVL[ENSG00000143748.13]
Back to top
Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr1 224430667 224435413 enh947 224518089 82676
chr1 224437445 224456975 enh12717 224518089 61114
chr1 224458940 224459060 vista5294 224518089 59029
chr1 224528791 224528972 vista5295 224518089 10702
chr1 224545542 224546006 vista5296 224518089 27453
chr1 224567685 224571835 enh948 224518089 49596
chr1 224593326 224597975 enh27576 224518089 75237
chr1 224598124 224598418 vista5297 224518089 80035
chr1 224613085 224617275 enh79404 224518089 94996

Transcript facotrs that regulate NVL[ENSG00000143748.13]
Back to top
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
chr1 223894405 rs144240965 T C 520631 Esophagus 0.795428 978099
chr1 224443776 rs7521015 T C 0 Heart 0.0619808 981082
chr1 224689573 rs373929343 G GCTCCTGGC 171484 Ovary 0.238439 982064
chr1 224776820 rs16849875 G A 258731 Uterus 0.376637 982600
chr1 224389444 rs74750827 A G 25592 Stomach 0.212465 980588

Genomic Location chr1:224415036-224518089[-]
TSS 224518089
Gene Name NVL
Ensembl ID ENSG00000143748.13
ENTREZID 4931
Uniprot
B4DF43
O15381
Protein Name
NVL protein
Nuclear VCP-like protein
Nuclear valosin-containing protein-like