Variant report

Variant	rs6853969
Chromosome Location	chr4:173654619-173654620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10014796	0.93[EUR][1000 genomes]
rs10029955	1.00[ASN][1000 genomes]
rs10031202	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10213357	0.95[EUR][1000 genomes]
rs10222748	0.93[EUR][1000 genomes]
rs1074144	1.00[ASN][1000 genomes]
rs11132960	0.95[EUR][1000 genomes]
rs11729518	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11730738	0.81[EUR][1000 genomes]
rs13134091	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13152161	1.00[ASN][1000 genomes]
rs1347703	0.84[ASN][1000 genomes]
rs1437843	1.00[ASN][1000 genomes]
rs1437844	1.00[ASN][1000 genomes]
rs1437845	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1455120	1.00[ASN][1000 genomes]
rs1540473	0.95[EUR][1000 genomes]
rs1595413	0.95[EUR][1000 genomes]
rs1837132	0.93[EUR][1000 genomes]
rs2196669	1.00[ASN][1000 genomes]
rs28552483	0.93[EUR][1000 genomes]
rs28579160	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28727534	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28767047	0.93[EUR][1000 genomes]
rs34364219	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35170073	0.93[EUR][1000 genomes]
rs6553640	1.00[ASN][1000 genomes]
rs6553648	0.95[EUR][1000 genomes]
rs67168311	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6822057	0.95[EUR][1000 genomes]
rs73869602	0.82[ASN][1000 genomes]
rs7669486	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7673000	1.00[ASN][1000 genomes]
rs7677835	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992901	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv880685	chr4:173562564-173661711	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv880613	chr4:173569281-173661711	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3327952	chr4:173591786-173805861	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173653200-173657400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:173654400-173656200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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