Variant report

Variant	rs73447043
Chromosome Location	chr15:76103076-76103077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs55923723	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58619115	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59596752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73449212	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531903	chr15:75889302-76342128	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv527186	chr15:75924443-76107730	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
3	nsv904397	chr15:76072030-76119092	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76093200-76108800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:76094600-76116400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:76094800-76106800	Weak transcription	Pancreas	Pancrea
4	chr15:76100400-76109200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:76102200-76103200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr15:76102200-76103200	Enhancers	HMEC	breast
7	chr15:76102200-76104000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:76102200-76104200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:76102600-76103200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr15:76102600-76103400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:76102600-76103600	Enhancers	Placenta	Placenta
12	chr15:76102800-76103400	Enhancers	NHEK	skin
13	chr15:76103000-76103200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:76103000-76103800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:76103000-76108200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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