Variant report

Variant	rs9862479
Chromosome Location	chr3:21586624-21586625
allele	C/T
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]
rs1841914	0.82[TSI][hapmap]
rs7647636	0.83[CEU][hapmap]
rs7648849	0.84[TSI][hapmap]
rs9881728	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv1006471	chr3:21385627-21596955	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1010460	chr3:21516810-21839871	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21561800-21587800	Weak transcription	Aorta	Aorta
2	chr3:21574000-21602000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:21584200-21587800	Active TSS	K562	blood
4	chr3:21585000-21601600	Weak transcription	Fetal Stomach	stomach
5	chr3:21585200-21589400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:21585400-21588600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:21585600-21586800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:21585800-21586800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:21585800-21602000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:21586000-21587000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:21586000-21589400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:21586200-21587000	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr3:21586600-21587200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:21586600-21587600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:21586600-21588400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:21586600-21588400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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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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