Variant report

Variant	rs6769840
Chromosome Location	chr3:19478182-19478183
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10428250	1.00[EUR][1000 genomes]
rs17005951	1.00[YRI][hapmap]
rs17005978	1.00[YRI][hapmap]
rs17005994	1.00[EUR][1000 genomes]
rs17006066	1.00[EUR][1000 genomes]
rs1837894	1.00[EUR][1000 genomes]
rs3905630	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs6549914	1.00[EUR][1000 genomes]
rs6805014	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7635253	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517847	chr3:18845347-19483695	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010123	chr3:18990307-19989504	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1004602	chr3:19031671-19930052	Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv536511	chr3:19031671-19930052	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv948636	chr3:19335802-19856585	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv589855	chr3:19409153-19512074	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3386719	chr3:19454588-19895807	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19472600-19479600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr3:19473000-19479000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:19473000-19491400	Weak transcription	Primary B cells from cord blood	blood
4	chr3:19473200-19479200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:19474400-19513200	Weak transcription	Brain Germinal Matrix	brain
6	chr3:19474600-19478400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr3:19474600-19482000	Weak transcription	Fetal Brain Male	brain
8	chr3:19474800-19479800	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:19477800-19479400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:19478000-19478400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:19478000-19478600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:19478000-19478600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:19478000-19478800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr3:19478000-19479600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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