Variant report

Variant	rs61185137
Chromosome Location	chr8:102930062-102930063
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11986127	1.00[EUR][1000 genomes]
rs11996557	0.94[EUR][1000 genomes]
rs11997578	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11997754	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868691	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868707	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868710	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16868711	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868715	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868730	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868739	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868741	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34561956	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35690650	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55754486	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55824424	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55897683	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55939093	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56047034	0.88[EUR][1000 genomes]
rs57350304	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58938702	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59217267	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59278862	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59332201	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61383411	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005622	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280871	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280876	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280878	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280879	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280880	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280885	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280888	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280891	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73280899	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282603	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282609	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282612	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282613	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282614	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282618	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73282620	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73290530	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73696550	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73696551	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73696560	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73696564	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73696586	1.00[EUR][1000 genomes]
rs7816729	0.94[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	nsv1018653	chr8:102818271-103009082	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539700	chr8:102818271-103009082	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102915200-102938800	Weak transcription	Aorta	Aorta
2	chr8:102916200-102932200	Weak transcription	Lung	lung
3	chr8:102916200-102942600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:102920600-102956600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr8:102921000-102930400	Weak transcription	NHDF-Ad	bronchial
6	chr8:102921200-102938200	Weak transcription	Ovary	ovary
7	chr8:102925000-102936600	Weak transcription	Fetal Heart	heart

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