Variant report

Variant	rs72631341
Chromosome Location	chr17:66806371-66806372
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:66678045..66679683-chr17:66805508..66807559,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11867232	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11869086	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs16967199	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16967205	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16967208	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16967215	0.86[AMR][1000 genomes]
rs16973309	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16973316	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57197545	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58039149	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59913929	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60553909	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61192710	0.93[ASN][1000 genomes]
rs6501742	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6501758	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6501759	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68139244	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7211767	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7211958	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7215386	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7218023	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7223634	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72631340	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72851036	0.86[AMR][1000 genomes]
rs72851039	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8069179	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8070095	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8070117	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8070228	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8078115	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9889514	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9889534	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9891717	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9895298	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9911308	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9911809	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9912257	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9916699	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv575927	chr17:66787428-66817866	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv908694	chr17:66802992-66913936	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66804400-66807000	Weak transcription	Liver	Liver
2	chr17:66804400-66809200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr17:66804400-66809200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr17:66804600-66808800	Weak transcription	NHDF-Ad	bronchial
5	chr17:66805000-66809200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr17:66805600-66806400	Enhancers	Fetal Lung	lung
7	chr17:66805600-66807000	Weak transcription	Fetal Stomach	stomach
8	chr17:66806000-66809200	Weak transcription	Adipose Nuclei	Adipose
9	chr17:66806000-66811600	Weak transcription	Right Atrium	heart
10	chr17:66806000-66817200	Weak transcription	Ovary	ovary

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