Variant report

Variant	rs11830159
Chromosome Location	chr12:59768390-59768391
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11832063	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11833678	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11835273	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11837506	0.93[EUR][1000 genomes]
rs12810255	0.86[EUR][1000 genomes]
rs12810370	0.82[EUR][1000 genomes]
rs12812247	0.86[EUR][1000 genomes]
rs12812349	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12812654	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12815892	0.93[EUR][1000 genomes]
rs12817396	0.86[EUR][1000 genomes]
rs12823449	0.89[EUR][1000 genomes]
rs12824894	0.82[EUR][1000 genomes]
rs12824908	0.89[EUR][1000 genomes]
rs12831896	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2203392	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34238449	0.82[EUR][1000 genomes]
rs34418591	0.87[EUR][1000 genomes]
rs34531399	0.82[EUR][1000 genomes]
rs35103945	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35337561	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35377390	0.89[EUR][1000 genomes]
rs35407860	0.82[EUR][1000 genomes]
rs35438740	0.87[EUR][1000 genomes]
rs35563376	0.87[EUR][1000 genomes]
rs35710665	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35715187	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35797812	0.86[EUR][1000 genomes]
rs36011226	0.86[EUR][1000 genomes]
rs36094921	0.86[EUR][1000 genomes]
rs4447211	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56179488	0.89[EUR][1000 genomes]
rs56376003	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs66861324	0.89[EUR][1000 genomes]
rs66931930	0.89[EUR][1000 genomes]
rs67042072	0.89[EUR][1000 genomes]
rs67534243	0.89[EUR][1000 genomes]
rs67600993	0.82[ASN][1000 genomes]
rs7134200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73120170	0.87[EUR][1000 genomes]
rs73120185	0.89[EUR][1000 genomes]
rs73121907	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7314663	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7484879	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7487998	0.86[EUR][1000 genomes]
rs7962767	0.87[EUR][1000 genomes]
rs7975333	0.82[EUR][1000 genomes]
rs982772	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv559052	chr12:59532203-59809256	Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2762982	chr12:59659871-60000135	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1042271	chr12:59668468-59993468	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv520767	chr12:59671388-59782228	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1038467	chr12:59680717-59999008	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv541507	chr12:59680717-59999008	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1049084	chr12:59700333-59993468	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv869425	chr12:59746898-60479741	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59767200-59776000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr12:59767600-59769600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:59767800-59776000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:59768000-59775000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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