Enhancers that regulate VWA5A[ENSG00000110002.11]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr11 123938205 123944335 enh103632 123986069 41734
chr11 123941712 123941923 vista11937 123986069 44146
chr11 123944625 123959475 enh14359 123986069 26594
chr11 123945702 123946055 vista11938 123986069 40014
chr11 123948297 123948692 vista11939 123986069 37377
chr11 123949311 123949466 vista11940 123986069 36603
chr11 123950495 123950749 vista11941 123986069 35320
chr11 123951200 123951810 vista11942 123986069 34259
chr11 123957354 123957540 vista11943 123986069 28529
chr11 123963965 123968755 enh74932 123986069 17314
chr11 123984777 123984974 vista11944 123986069 1095
chr11 123992941 123993165 vista11945 123986069 6872
chr11 124042805 124050255 enh101285 123986069 56736
chr11 124048157 124048385 vista11946 123986069 62088
chr11 124059545 124068115 enh51047 123986069 73476
chr11 124062644 124062948 vista11947 123986069 76575
chr11 124071765 124075915 enh90918 123986069 85696
chr11 124076185 124080335 enh90919 123986069 90116

Transcript facotrs that regulate VWA5A[ENSG00000110002.11]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
chr11 123984524 123985074 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 123986069 995 108005243
chr11 123984837 123984852 HNF4A JASPAR yes 123986069 1217 114149185
chr11 123984838 123984852 NR2F1 JASPAR yes 123986069 1217 114149186
chr11 123984838 123984853 HNF4G JASPAR yes 123986069 1216 114149187
chr11 123984838 123984853 NR2C2 JASPAR yes 123986069 1216 114149188
chr11 123984868 123984874 TCF4 TRANSFAC yes 123986069 1195 114149189
chr11 123984883 123984898 NFYB JASPAR yes 123986069 1171 114149190
chr11 123984885 123984901 NFYA JASPAR yes 123986069 1168 114149191
chr11 123984890 123984894 H1TF2 TRANSFAC yes 123986069 1175 114149192
chr11 123984890 123984894 NFE TRANSFAC yes 123986069 1175 114149193
chr11 123984890 123984894 SRF TRANSFAC yes 123986069 1175 114149194
chr11 123984892 123984902 NFATC3 JASPAR yes 123986069 1167 114149195
chr11 123984914 123984919 ETS2 TRANSFAC yes 123986069 1150 114149196
chr11 123984933 123984938 H4TF1 TRANSFAC yes 123986069 1131 114149197
chr11 123984938 123984949 EBF1 JASPAR yes 123986069 1120 114149198
chr11 123984952 123984957 GATA2 JASPAR yes 123986069 1112 114149199
chr11 123984957 123984965 FEV JASPAR yes 123986069 1104 114149200
chr11 123984959 123984966 SPIB JASPAR yes 123986069 1103 114149201

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr11 123002400 rs35894287 TG T 983669 Esophagus 0.136718 2328659
chr11 123293657 rs398045684 TC T 692412 Esophagus 0.0140892 2332137
chr11 124078704 rs11219499 G A 60276 Lung 0.135275 2335741

Genomic Location chr11:123986069-124018428[+]
TSS 123986069
Gene Name VWA5A
Ensembl ID ENSG00000110002.11
ENTREZID 4013
Uniprot
O00534
A0A024R3H3
Protein Name
highly similar to Loss of heterozygosity 11 chromosomal region 2 gene A protein
cDNA FLJ55206
von Willebrand factor A domain-containing protein 5A