Variant report

Variant	rs6814145
Chromosome Location	chr4:167260001-167260002
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1350654	0.82[EUR][1000 genomes]
rs1531338	0.82[EUR][1000 genomes]
rs1663605	0.82[EUR][1000 genomes]
rs1663606	0.82[EUR][1000 genomes]
rs1675012	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1675016	0.82[EUR][1000 genomes]
rs1675018	0.82[EUR][1000 genomes]
rs1675032	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1870532	0.82[EUR][1000 genomes]
rs28760893	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs364832	0.89[EUR][1000 genomes]
rs368067	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs370093	0.82[EUR][1000 genomes]
rs373801	0.89[EUR][1000 genomes]
rs382617	0.82[EUR][1000 genomes]
rs386236	0.89[EUR][1000 genomes]
rs386265	0.89[EUR][1000 genomes]
rs390012	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs394704	0.89[EUR][1000 genomes]
rs399138	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs408059	0.82[EUR][1000 genomes]
rs410627	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs410691	0.82[EUR][1000 genomes]
rs412193	0.89[EUR][1000 genomes]
rs413764	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs419857	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs421201	0.82[EUR][1000 genomes]
rs423947	0.82[EUR][1000 genomes]
rs424343	0.82[EUR][1000 genomes]
rs426538	0.89[EUR][1000 genomes]
rs427837	0.82[EUR][1000 genomes]
rs431882	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs434957	0.89[EUR][1000 genomes]
rs435102	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs443289	0.89[EUR][1000 genomes]
rs443475	0.82[EUR][1000 genomes]
rs445070	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs445668	0.89[EUR][1000 genomes]
rs446918	0.89[EUR][1000 genomes]
rs452467	0.89[EUR][1000 genomes]
rs576300	0.89[EUR][1000 genomes]
rs6837241	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs692298	0.89[EUR][1000 genomes]
rs833486	0.86[AMR][1000 genomes];0.89[EUR][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	nsv821638	chr4:166837633-167262625	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1034421	chr4:166961339-167893289	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537339	chr4:166961339-167893289	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv881029	chr4:167060016-167284757	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1032009	chr4:167154813-167403235	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv880900	chr4:167155443-167368812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv881290	chr4:167163302-167284757	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv880804	chr4:167185391-167274823	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv880967	chr4:167185391-167366567	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv881405	chr4:167193885-167628013	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167256800-167261600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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