Variant report

Variant	rs56262782
Chromosome Location	chr9:101030586-101030587
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10115971	0.91[ASN][1000 genomes]
rs10123643	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10124977	0.91[ASN][1000 genomes]
rs10760216	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10760217	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10760218	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818627	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818640	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818644	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818645	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818646	0.86[ASN][1000 genomes]
rs10818648	0.84[ASN][1000 genomes]
rs10818656	0.84[ASN][1000 genomes]
rs10818658	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818662	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818666	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818672	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10818676	0.84[ASN][1000 genomes]
rs10818677	0.84[ASN][1000 genomes]
rs10818678	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10818689	0.89[ASN][1000 genomes]
rs10818690	0.89[ASN][1000 genomes]
rs10818691	0.91[ASN][1000 genomes]
rs10818692	0.96[ASN][1000 genomes]
rs10818693	0.96[ASN][1000 genomes]
rs10818739	0.82[ASN][1000 genomes]
rs10818743	0.81[ASN][1000 genomes]
rs10985583	0.84[ASN][1000 genomes]
rs10985634	0.89[ASN][1000 genomes]
rs10985641	0.96[ASN][1000 genomes]
rs10985642	0.96[ASN][1000 genomes]
rs10985653	0.96[ASN][1000 genomes]
rs10985669	0.96[ASN][1000 genomes]
rs10985680	0.96[ASN][1000 genomes]
rs10985689	0.96[ASN][1000 genomes]
rs10985711	0.96[ASN][1000 genomes]
rs10985720	0.96[ASN][1000 genomes]
rs10985743	0.94[ASN][1000 genomes]
rs10985745	0.94[ASN][1000 genomes]
rs10985757	0.82[ASN][1000 genomes]
rs10985765	0.81[ASN][1000 genomes]
rs10985772	0.81[ASN][1000 genomes]
rs12237988	0.84[ASN][1000 genomes]
rs12346750	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1435253	0.82[ASN][1000 genomes]
rs1435257	0.90[ASN][1000 genomes]
rs1573024	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1573025	0.84[ASN][1000 genomes]
rs17766883	0.84[ASN][1000 genomes]
rs17766913	0.84[ASN][1000 genomes]
rs1935389	0.84[ASN][1000 genomes]
rs2900380	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4379551	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4742719	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4742721	0.96[ASN][1000 genomes]
rs4742722	0.96[ASN][1000 genomes]
rs4743187	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4743192	0.84[ASN][1000 genomes]
rs5010004	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62574277	0.84[ASN][1000 genomes]
rs62574288	0.96[ASN][1000 genomes]
rs62574300	0.96[ASN][1000 genomes]
rs6478631	0.84[ASN][1000 genomes]
rs7032046	0.84[ASN][1000 genomes]
rs7853847	0.80[ASN][1000 genomes]
rs7859655	0.96[ASN][1000 genomes]
rs7873849	0.84[ASN][1000 genomes]
rs7874856	0.96[ASN][1000 genomes]
rs879368	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9696283	0.83[ASN][1000 genomes]
rs9802466	0.84[ASN][1000 genomes]
rs9802650	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1045780	chr9:100943318-101080389	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv540180	chr9:100943318-101080389	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv519818	chr9:101024887-101092316	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	esv3394263	chr9:101027594-101033575	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv3442012	chr9:101027638-101033547	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3521792	chr9:101027681-101033515	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv3521793	chr9:101027681-101033515	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101026400-101036000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:101027800-101031200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:101028200-101037000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:101028400-101031200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr9:101028400-101033600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr9:101028400-101033800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:101028400-101033800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:101030000-101030600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr9:101030000-101031400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr9:101030400-101032200	Weak transcription	Hela-S3	cervix

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