Variant report

Variant	rs16919833
Chromosome Location	chr11:93756866-93756867
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16919687	1.00[AMR][1000 genomes]
rs16919769	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16919800	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16919804	1.00[AMR][1000 genomes]
rs16919868	1.00[AMR][1000 genomes]
rs71480697	1.00[AMR][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:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93752200-93758000	Weak transcription	NH-A	brain
2	chr11:93755000-93757400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:93755600-93760600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:93755800-93761200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:93756200-93757000	Enhancers	NHEK	skin
6	chr11:93756200-93759000	Enhancers	HMEC	breast
7	chr11:93756600-93758000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:93756800-93757000	Active TSS	Esophagus	oesophagus
9	chr11:93756800-93757200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:93756800-93757600	Enhancers	Fetal Kidney	kidney
11	chr11:93756800-93758000	Enhancers	K562	blood

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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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