Variant report

Variant	rs1792329
Chromosome Location	chr11:71111182-71111183
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1372109	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs1621818	0.83[EUR][1000 genomes]
rs1626847	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1626891	0.83[EUR][1000 genomes]
rs1628926	0.84[EUR][1000 genomes]
rs1660837	0.82[EUR][1000 genomes]
rs1660838	0.83[EUR][1000 genomes]
rs1660839	0.83[EUR][1000 genomes]
rs1660840	0.83[EUR][1000 genomes]
rs1660841	0.83[EUR][1000 genomes]
rs1660842	0.83[EUR][1000 genomes]
rs1660849	0.83[EUR][1000 genomes]
rs1660850	0.83[EUR][1000 genomes]
rs1660872	0.82[EUR][1000 genomes]
rs1660881	0.82[EUR][1000 genomes]
rs1660888	0.82[EUR][1000 genomes]
rs1660894	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1790308	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1790313	0.84[EUR][1000 genomes]
rs1790320	0.83[EUR][1000 genomes]
rs1792220	0.83[EUR][1000 genomes]
rs1792255	0.83[EUR][1000 genomes]
rs1792258	0.82[EUR][1000 genomes]
rs1792261	0.82[EUR][1000 genomes]
rs1792300	0.82[EUR][1000 genomes]
rs1792308	0.82[EUR][1000 genomes]
rs1792309	0.82[EUR][1000 genomes]
rs1792310	0.82[EUR][1000 genomes]
rs1792335	0.84[EUR][1000 genomes]
rs3133258	0.94[CEU][hapmap]
rs877246	0.89[CEU][hapmap];0.82[EUR][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	nsv1048123	chr11:70795222-71231382	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
2	nsv832202	chr11:71088949-71131368	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv526973	chr11:71088949-71215880	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv897897	chr11:71088949-71217571	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
6	nsv897898	chr11:71103143-71211654	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv519224	chr11:71108341-71215880	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 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	chr11:71102800-71114000	Weak transcription	Pancreas	Pancrea
2	chr11:71105000-71111400	Weak transcription	Spleen	Spleen
3	chr11:71110600-71113800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:71110800-71111400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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