Variant report

Variant	rs58773763
Chromosome Location	chr5:111868292-111868293
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]
rs11749928	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11951455	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12655349	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56317607	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58871758	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6889110	0.83[AMR][1000 genomes];0.93[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	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv882715	chr5:111836278-111894491	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
3	nsv882716	chr5:111848890-111894491	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111862400-111868400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:111865400-111868400	Weak transcription	Adipose Nuclei	Adipose
3	chr5:111865600-111869000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:111865600-111869800	Weak transcription	K562	blood
5	chr5:111867800-111870800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr5:111868000-111868600	Flanking Active TSS	Primary B cells from peripheral blood	blood
7	chr5:111868000-111868600	Enhancers	GM12878-XiMat	blood
8	chr5:111868000-111868800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr5:111868000-111869600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:111868000-111870400	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr5:111868200-111868600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:111868200-111869400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:111868200-111869600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr5:111868200-111869800	Enhancers	Primary B cells from cord blood	blood
15	chr5:111868200-111870000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:111868200-111870200	Enhancers	Primary Natural Killer cells fromperipheralblood	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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