Variant report

Variant	rs73382010
Chromosome Location	chr12:86345015-86345016
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10047659	0.84[ASN][1000 genomes]
rs10083080	0.84[ASN][1000 genomes]
rs10746355	0.85[ASN][1000 genomes]
rs10746356	0.85[ASN][1000 genomes]
rs10746357	0.85[ASN][1000 genomes]
rs10779218	0.85[ASN][1000 genomes]
rs10779219	0.85[ASN][1000 genomes]
rs10779222	0.85[ASN][1000 genomes]
rs10863100	0.87[ASN][1000 genomes]
rs10863115	0.85[ASN][1000 genomes]
rs10863117	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10863118	0.85[ASN][1000 genomes]
rs10863119	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10863120	0.85[ASN][1000 genomes]
rs10863123	0.85[ASN][1000 genomes]
rs11117094	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11117108	0.85[ASN][1000 genomes]
rs11117109	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11117116	0.85[ASN][1000 genomes]
rs11117117	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11117120	0.85[ASN][1000 genomes]
rs11117121	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11117123	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11117125	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11117128	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11829570	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12099914	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12231117	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12231763	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1374995	0.89[ASN][1000 genomes]
rs1448093	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1448094	0.85[ASN][1000 genomes]
rs1584367	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2044617	0.85[ASN][1000 genomes]
rs2044618	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2044619	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2121892	0.84[ASN][1000 genomes]
rs2405627	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2405789	0.85[ASN][1000 genomes]
rs4919775	0.85[ASN][1000 genomes]
rs61929387	0.86[ASN][1000 genomes]
rs6539934	0.85[ASN][1000 genomes]
rs7134573	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7134915	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7301496	0.85[ASN][1000 genomes]
rs7305284	0.85[ASN][1000 genomes]
rs7305891	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7313443	0.85[ASN][1000 genomes]
rs7960313	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7972238	0.85[ASN][1000 genomes]
rs7974794	0.85[ASN][1000 genomes]
rs7978132	0.85[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	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv1797806	chr12:86198935-86425608	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv559667	chr12:86318004-86416212	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86343000-86346200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:86343200-86345600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr12:86343200-86346600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr12:86343600-86345800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr12:86343600-86346600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:86343600-86348000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr12:86343600-86348200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:86343800-86347000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr12:86344400-86345600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:86344600-86345400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr12:86344800-86345200	Weak transcription	H1 Cell Line	embryonic stem cell

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