Enhancers that regulate HMGN2[ENSG00000198830.6]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr1 26710165 26717815 enh11652 26798941 81126
chr1 26735858 26736255 vista871 26798941 62686
chr1 26738740 26738942 vista872 26798941 59999
chr1 26739065 26739644 vista873 26798941 59297
chr1 26741479 26747975 enh11653 26798941 50966
chr1 26745463 26745863 vista874 26798941 53078
chr1 26805925 26816635 enh11654 26798941 6984
chr1 26824345 26830235 enh162 26798941 25404
chr1 26827232 26827869 vista875 26798941 28291
chr1 26834985 26839355 enh101100 26798941 36044
chr1 26844889 26849191 enh86792 26798941 45948
chr1 26857367 26871235 enh163 26798941 58426

Transcript facotrs that regulate HMGN2[ENSG00000198830.6]
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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
chr1 26829582 rs6598968 A G 27119 Esophagus 0.00129931 180556
chr1 26832460 rs7519883 A G 29997 Esophagus 0.00938436 180584
chr1 26913951 rs79521556 A G 111488 Esophagus 0.706311 181112
chr1 26114310 rs6690756 C G 684631 Heart 0.365273 175959
chr1 26715872 rs78631043 A C 83069 Heart 0.328872 179878
chr1 26009250 rs2786878 T C 789691 Pancreas 0.166024 175108
chr1 26858353 rs12118996 C T 55890 Breast 0.19405 180804
chr1 26284217 rs139941686 G A,C 514724 Spleen 0.242446 177395
chr1 26092014 rs139643627 CTG C 706927 Thyroid 0.00762073 175832
chr1 26008770 rs148501216 G A 790171 Liver 0.00387916 175105
chr1 26805169 rs2925523 C T 2706 Stomach 0.284783 180367
chr1 25943096 rs141258614 G A,T 855845 Adrenal 0.33007 174411

Genomic Location chr1:26798941-26802463[+]
TSS 26798941
Gene Name HMGN2
Ensembl ID ENSG00000198830.6
ENTREZID 3151
Uniprot
P05204
Protein Name
isoform CRA_a
High-mobility group nucleosomal binding domain 2
Non-histone chromosomal protein HMG-17