Variant report

Variant	rs10922068
Chromosome Location	chr1:196406715-196406716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10494743	0.89[EUR][1000 genomes]
rs10737670	0.86[ASN][1000 genomes]
rs10754187	0.92[ASN][1000 genomes]
rs10754188	0.85[EUR][1000 genomes]
rs10801530	0.88[ASN][1000 genomes]
rs10801531	0.88[ASN][1000 genomes]
rs10801532	0.88[ASN][1000 genomes]
rs10801533	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10801534	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10801535	0.96[ASN][1000 genomes]
rs10801538	0.89[EUR][1000 genomes]
rs10922066	0.96[ASN][1000 genomes]
rs10922067	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10922073	0.87[EUR][1000 genomes]
rs11576790	0.84[EUR][1000 genomes]
rs12049567	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12065519	0.84[EUR][1000 genomes]
rs12069983	0.95[ASN][1000 genomes]
rs12069990	0.95[ASN][1000 genomes]
rs12121250	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12729649	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12738109	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1416962	0.87[EUR][1000 genomes]
rs1538684	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1538685	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1538686	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1538687	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1769996	0.85[ASN][1000 genomes]
rs2027368	0.85[ASN][1000 genomes]
rs2147469	0.85[ASN][1000 genomes]
rs2878557	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2878558	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2878559	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35582782	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3855964	0.95[ASN][1000 genomes]
rs3927686	0.95[ASN][1000 genomes]
rs3928857	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6678457	0.95[ASN][1000 genomes]
rs6696801	0.89[EUR][1000 genomes]
rs7515074	0.81[ASN][1000 genomes]
rs7515472	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7531611	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7535696	0.88[ASN][1000 genomes]
rs7550015	0.95[ASN][1000 genomes]
rs7551077	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9427622	0.80[ASN][1000 genomes]
rs946750	0.86[ASN][1000 genomes]
rs9659527	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469680	chr1:196259846-196419016	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv482746	chr1:196259846-196419016	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv931415	chr1:196270759-196744780	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv872953	chr1:196286639-196411281	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1009233	chr1:196301712-196568874	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	nsv872956	chr1:196339655-196411281	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv872957	chr1:196347066-196411281	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv3409802	chr1:196402929-196408127	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3407926	chr1:196405154-196407902	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3362394	chr1:196405354-196407502	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196395200-196416400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:196398000-196407200	Weak transcription	Liver	Liver
3	chr1:196401600-196416400	Weak transcription	Ovary	ovary

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