Variant report

Variant	rs6922125
Chromosome Location	chr6:4772598-4772599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs60731840	0.86[EUR][1000 genomes]
rs62384841	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62384844	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62384845	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62384848	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62384852	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62384853	0.86[EUR][1000 genomes]
rs62384855	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6907313	0.83[EUR][1000 genomes]
rs6908435	0.83[EUR][1000 genomes]
rs6921417	0.88[EUR][1000 genomes]
rs6927577	0.83[EUR][1000 genomes]
rs7752474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9502236	0.82[EUR][1000 genomes]
rs9502237	0.81[EUR][1000 genomes]
rs9504248	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv3429586	chr6:4719363-4792438	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1017938	chr6:4729592-4774914	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4761000-4773200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:4769800-4775000	Weak transcription	Aorta	Aorta
3	chr6:4771600-4772600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:4771600-4772800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr6:4771600-4773000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:4771800-4772600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr6:4771800-4772600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:4771800-4772600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:4771800-4772600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr6:4772000-4772600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:4772000-4772800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr6:4772000-4773000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr6:4772200-4773200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr6:4772400-4772600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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

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