Variant report

Variant	rs59368900
Chromosome Location	chr4:133056725-133056726
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10009200	0.96[ASN][1000 genomes]
rs10019344	0.95[ASN][1000 genomes]
rs10033560	0.97[ASN][1000 genomes]
rs10461213	0.83[AFR][1000 genomes]
rs11930158	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12054493	0.87[AFR][1000 genomes]
rs13107581	0.96[ASN][1000 genomes]
rs13117543	0.92[ASN][1000 genomes]
rs13124410	0.90[ASN][1000 genomes]
rs13127678	0.96[ASN][1000 genomes]
rs13137404	0.96[ASN][1000 genomes]
rs13141865	0.86[ASN][1000 genomes]
rs13152802	0.93[ASN][1000 genomes]
rs17047796	0.96[ASN][1000 genomes]
rs1827740	0.96[ASN][1000 genomes]
rs2418555	0.81[AFR][1000 genomes]
rs60692721	0.89[AMR][1000 genomes]
rs62320262	0.81[AFR][1000 genomes]
rs62320263	0.80[AFR][1000 genomes]
rs62320264	0.80[AFR][1000 genomes]
rs6831366	0.90[ASN][1000 genomes]
rs7660282	0.96[ASN][1000 genomes]
rs7660499	0.95[ASN][1000 genomes]
rs7661243	0.96[ASN][1000 genomes]
rs7661355	0.96[ASN][1000 genomes]
rs7666320	0.96[ASN][1000 genomes]
rs7680111	0.93[ASN][1000 genomes]
rs7680265	0.88[ASN][1000 genomes]
rs9790555	0.97[ASN][1000 genomes]
rs9990622	0.93[ASN][1000 genomes]
rs9996530	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470073	chr4:132902055-133101094	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1031888	chr4:132903485-133355824	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv880002	chr4:132970231-133082999	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv595445	chr4:133022641-133338765	Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv880003	chr4:133047300-133513991	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133048200-133066600	Weak transcription	ES-UCSF4 Cell Line	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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