Variant report

Variant	rs7900724
Chromosome Location	chr10:28147799-28147800
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10826355	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10826356	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11006747	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006749	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11006750	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12780619	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1556641	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1556642	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1857617	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2065687	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2065688	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3897931	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3901839	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4747606	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4747607	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4749266	0.88[ASN][1000 genomes]
rs4749272	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7077304	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7896104	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831813	chr10:28017606-28200651	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv971859	chr10:28070066-28271252	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv550283	chr10:28144330-28167326	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28121000-28158600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:28141200-28153800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr10:28144800-28152600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:28147200-28149400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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

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