Variant report

Variant	rs9834688
Chromosome Location	chr3:85035279-85035280
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1016305	0.81[ASN][1000 genomes]
rs1016306	0.84[ASN][1000 genomes]
rs1248857	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1248860	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1872553	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4301023	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6768455	0.86[EUR][1000 genomes]
rs7651996	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9816652	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9831123	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9833081	0.86[EUR][1000 genomes]
rs9836888	0.86[EUR][1000 genomes]
rs9840607	0.84[ASN][1000 genomes]
rs9871198	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1001316	chr3:84773522-85071342	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv877091	chr3:84876250-85069287	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv1829788	chr3:84926769-85086403	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1000793	chr3:85020452-85051839	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85029400-85036600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr3:85030000-85036200	Weak transcription	Fetal Lung	lung
3	chr3:85031200-85036200	Weak transcription	Brain Anterior Caudate	brain
4	chr3:85032000-85037800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:85032800-85035600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:85033600-85036200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr3:85033800-85035400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:85033800-85035600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:85033800-85036600	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:85034000-85035400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr3:85034200-85036600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr3:85034200-85040400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr3:85034200-85042600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr3:85034200-85048200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:85034600-85035600	Enhancers	Brain Substantia Nigra	brain
16	chr3:85035000-85037000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr3:85035200-85036200	Weak transcription	Brain Angular Gyrus	brain
18	chr3:85035200-85041000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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

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