Variant report

Variant	rs6865572
Chromosome Location	chr5:108401245-108401246
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10043207	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10061864	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10062069	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10066497	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10477434	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10477435	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10515399	0.83[JPT][hapmap]
rs11240990	0.89[ASN][1000 genomes]
rs11948270	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs11948684	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11951285	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs11951595	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11955924	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs11958129	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11960400	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs12153527	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs12153646	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs13355279	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13357674	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1366081	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17534396	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs1896582	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2416196	1.00[CHB][hapmap];0.90[JPT][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2416197	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3797819	0.83[JPT][hapmap]
rs3797820	0.83[JPT][hapmap]
rs3797823	0.83[JPT][hapmap]
rs3797825	0.82[JPT][hapmap]
rs3797832	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3797833	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3797834	0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs3797837	1.00[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs3797847	0.90[JPT][hapmap]
rs3822684	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs3822685	0.91[JPT][hapmap]
rs4957793	0.83[JPT][hapmap]
rs60777927	0.98[ASN][1000 genomes]
rs6872299	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs6882698	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs6882759	0.83[JPT][hapmap]
rs6883750	1.00[JPT][hapmap]
rs6884133	0.91[JPT][hapmap]
rs6893501	0.90[JPT][hapmap]
rs6893738	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72790597	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72790598	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72790599	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72790602	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72792507	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7702557	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs7714599	0.89[JPT][hapmap]
rs7718925	0.90[JPT][hapmap]
rs7729380	0.91[JPT][hapmap]
rs7732335	0.83[JPT][hapmap]
rs7733971	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs7734092	0.83[JPT][hapmap]
rs7734110	0.83[JPT][hapmap]
rs7734437	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs7735749	0.83[JPT][hapmap]
rs9885203	0.85[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[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	nsv830443	chr5:108326491-108496723	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv882692	chr5:108391660-108474166	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv882693	chr5:108391660-108502493	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882694	chr5:108391660-108524416	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 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	chr5:108360400-108404800	Weak transcription	Colon Smooth Muscle	Colon
2	chr5:108360400-108425200	Weak transcription	Aorta	Aorta
3	chr5:108388200-108401800	Weak transcription	Ovary	ovary
4	chr5:108388800-108412000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:108390600-108401600	Weak transcription	HSMMtube	muscle
6	chr5:108401200-108401400	Enhancers	Gastric	stomach
7	chr5:108401200-108402600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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