Enhancers that regulate LIN7B[ENSG00000104863.7]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr19 49521043 49521282 vista29759 49617581 96299
chr19 49524183 49524468 vista29760 49617581 93113
chr19 49577003 49577438 vista29761 49617581 40143
chr19 49590520 49590786 vista29762 49617581 26795
chr19 49596327 49600684 enh44673 49617581 16897
chr19 49626565 49630715 enh18140 49617581 8984
chr19 49644265 49651332 enh89951 49617581 26684
chr19 49663180 49667330 enh101566 49617581 45599
chr19 49678182 49682692 enh32973 49617581 60601
chr19 49687505 49691655 enh92844 49617581 69924
chr19 49690208 49690571 vista29763 49617581 72627
chr19 49698080 49698342 vista29764 49617581 80499
chr19 49705299 49713415 enh32974 49617581 87718
chr19 49710890 49711280 vista29765 49617581 93309
chr19 49715212 49723108 enh44674 49617581 97631

Transcript facotrs that regulate LIN7B[ENSG00000104863.7]
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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

Genomic Location chr19:49617581-49621717[+]
TSS 49617581
Gene Name LIN7B
Ensembl ID ENSG00000104863.7
ENTREZID 64130
Uniprot
Q9HAP6
Protein Name
Protein lin-7 homolog B