Variant report

Variant	rs9348577
Chromosome Location	chr6:23610946-23610947
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs34711657	0.94[ASN][1000 genomes]
rs4389758	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs489884	0.84[ASN][1000 genomes]
rs497731	0.84[ASN][1000 genomes]
rs508408	0.80[ASN][1000 genomes]
rs521036	0.81[ASN][1000 genomes]
rs541604	0.84[ASN][1000 genomes]
rs565366	0.84[ASN][1000 genomes]
rs9348578	0.94[ASN][1000 genomes]
rs9348579	0.83[ASN][1000 genomes]
rs9379524	0.94[ASN][1000 genomes]
rs9393421	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9466858	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv830608	chr6:23558655-23644405	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23609800-23612000	Weak transcription	Fetal Lung	lung
2	chr6:23610000-23618600	Weak transcription	Fetal Kidney	kidney

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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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