Variant report

Variant	rs7944971
Chromosome Location	chr11:93759212-93759213
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1945782	1.00[EUR][1000 genomes]
rs2251782	1.00[EUR][1000 genomes]
rs2460068	1.00[EUR][1000 genomes]
rs2511408	1.00[EUR][1000 genomes]
rs58116509	1.00[EUR][1000 genomes]
rs59276869	1.00[EUR][1000 genomes]
rs60611834	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61285551	1.00[EUR][1000 genomes]
rs7113934	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73551201	1.00[EUR][1000 genomes]
rs73552919	1.00[EUR][1000 genomes]
rs73561150	1.00[EUR][1000 genomes]
rs73561172	1.00[EUR][1000 genomes]
rs73563050	1.00[EUR][1000 genomes]
rs73564781	1.00[EUR][1000 genomes]
rs73564788	1.00[EUR][1000 genomes]
rs73566804	1.00[EUR][1000 genomes]
rs73566811	1.00[EUR][1000 genomes]
rs73566818	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73566826	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73566837	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73566842	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73566869	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73568841	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73568844	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73568854	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73568863	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7928328	1.00[EUR][1000 genomes]
rs7940306	1.00[AFR][1000 genomes];1.00[EUR][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	nsv1049467	chr11:93651025-93778717	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv898183	chr11:93725384-93906735	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv898184	chr11:93741612-93969726	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93755600-93760600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:93755800-93761200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:93757400-93759400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:93758000-93760600	Weak transcription	Fetal Lung	lung
5	chr11:93758000-93760800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:93758800-93759400	Enhancers	NH-A	brain
7	chr11:93758800-93760200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:93759000-93760400	Weak transcription	HMEC	breast
9	chr11:93759200-93760400	ZNF genes & repeats	NHEK	skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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