Variant report

Variant	rs58559187
Chromosome Location	chr2:151130988-151130989
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10930047	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11890848	1.00[ASN][1000 genomes]
rs12105156	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12105546	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55752244	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56812074	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61440562	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004268	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004270	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004271	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004272	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004273	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004276	1.00[ASN][1000 genomes]
rs73004278	1.00[ASN][1000 genomes]
rs73004279	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73004280	1.00[ASN][1000 genomes]
rs73004285	1.00[ASN][1000 genomes]
rs7558183	0.87[AMR][1000 genomes];1.00[ASN][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	nsv995119	chr2:150556150-151294696	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1001838	chr2:150819672-151745876	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv535980	chr2:150819672-151745876	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 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	chr2:151113000-151138400	Weak transcription	Liver	Liver
2	chr2:151127800-151131200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:151128000-151138400	Weak transcription	Psoas Muscle	Psoas
4	chr2:151129400-151131000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:151129600-151136000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:151130000-151131200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:151130200-151131200	Enhancers	NHDF-Ad	bronchial
8	chr2:151130400-151131000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:151130600-151131200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:151130600-151131200	Enhancers	NHEK	skin
11	chr2:151130800-151133000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	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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