Variant report

Variant	rs61132425
Chromosome Location	chr11:63213128-63213129
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs60333825	1.00[AMR][1000 genomes]
rs60760957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7106014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485838	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485839	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485855	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485864	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485869	1.00[AMR][1000 genomes]
rs73488013	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7929031	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	esv1822068	chr11:63146055-63239984	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv3434037	chr11:63170556-63217699	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv350	chr11:63194122-63213673	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63212600-63214200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:63212800-63213400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:63213000-63213400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr11:63213000-63213400	Enhancers	HSMMtube	muscle
5	chr11:63213000-63213400	Enhancers	NHDF-Ad	bronchial
6	chr11:63213000-63213600	Enhancers	Osteobl	bone
7	chr11:63213000-63213800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:63213000-63214200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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Input of quick search could be:

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

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