Variant report

Variant	rs35582782
Chromosome Location	chr1:196399232-196399233
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10494743	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10754187	0.80[ASN][1000 genomes]
rs10754188	0.81[ASN][1000 genomes]
rs10801533	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10801534	0.84[ASN][1000 genomes]
rs10801535	0.84[ASN][1000 genomes]
rs10801537	0.80[ASN][1000 genomes]
rs10801538	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10801539	0.80[ASN][1000 genomes]
rs10922066	0.84[ASN][1000 genomes]
rs10922067	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10922068	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10922073	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11807331	0.80[ASN][1000 genomes]
rs12049567	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12069983	0.84[ASN][1000 genomes]
rs12069990	0.84[ASN][1000 genomes]
rs12121250	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12729649	0.84[ASN][1000 genomes]
rs12738109	0.84[ASN][1000 genomes]
rs12756143	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1416962	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1538684	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538685	0.84[ASN][1000 genomes]
rs1538686	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538687	0.83[ASN][1000 genomes]
rs2878557	0.84[ASN][1000 genomes]
rs2878558	0.84[ASN][1000 genomes]
rs2878559	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3855964	0.84[ASN][1000 genomes]
rs3927686	0.84[ASN][1000 genomes]
rs3928857	0.84[ASN][1000 genomes]
rs6428337	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6678457	0.84[ASN][1000 genomes]
rs6696801	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7515074	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7515472	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7527415	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7531611	0.84[ASN][1000 genomes]
rs7550015	0.83[ASN][1000 genomes]
rs7551077	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9427622	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9659527	0.86[EUR][1000 genomes];0.84[ASN][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	nsv469680	chr1:196259846-196419016	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv482746	chr1:196259846-196419016	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv931415	chr1:196270759-196744780	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv872953	chr1:196286639-196411281	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1009233	chr1:196301712-196568874	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	nsv872956	chr1:196339655-196411281	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv872957	chr1:196347066-196411281	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196377600-196403200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr1:196377800-196402800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:196378200-196400200	Weak transcription	Fetal Kidney	kidney
4	chr1:196387200-196403200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:196389600-196401200	Weak transcription	Fetal Muscle Leg	muscle
6	chr1:196391600-196403000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:196394600-196401000	Weak transcription	Ovary	ovary
8	chr1:196394800-196401200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:196395200-196400600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr1:196395200-196416400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:196397000-196400400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:196398000-196401200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:196398000-196407200	Weak transcription	Liver	Liver

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