Variant report

Variant	rs73018859
Chromosome Location	chr6:165354231-165354232
allele	A/G
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:12)

rs_ID	r²[population]
rs11751918	0.84[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs11759480	0.87[EUR][1000 genomes]
rs1923384	0.83[ASN][1000 genomes]
rs2146032	0.83[ASN][1000 genomes]
rs55717046	0.87[EUR][1000 genomes]
rs56316541	0.87[EUR][1000 genomes]
rs73018838	0.93[EUR][1000 genomes]
rs73018857	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73020990	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73020992	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73021001	0.80[EUR][1000 genomes]
rs73033259	0.87[EUR][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	nsv605232	chr6:164994771-165401154	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv886925	chr6:165319631-165705488	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr6:165350800-165356200	Weak transcription	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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