Variant report

Variant	rs6535377
Chromosome Location	chr4:76315076-76315077
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10011057	0.82[AMR][1000 genomes]
rs1020943	0.83[AMR][1000 genomes]
rs11728873	0.82[AMR][1000 genomes]
rs11728883	0.85[AMR][1000 genomes]
rs11731486	0.82[AMR][1000 genomes]
rs11731489	0.82[AMR][1000 genomes]
rs11731532	0.82[AMR][1000 genomes]
rs11938541	0.84[AMR][1000 genomes]
rs11941369	0.84[AMR][1000 genomes]
rs11941411	0.84[AMR][1000 genomes]
rs11941569	0.84[AMR][1000 genomes]
rs11941572	0.84[AMR][1000 genomes]
rs1466440	0.82[AMR][1000 genomes]
rs1466441	0.82[AMR][1000 genomes]
rs1532893	0.80[AMR][1000 genomes]
rs1808023	0.80[AMR][1000 genomes]
rs1873971	0.84[AMR][1000 genomes]
rs28401366	0.81[AMR][1000 genomes]
rs28433848	0.80[AMR][1000 genomes]
rs28440049	0.82[AMR][1000 genomes]
rs28510744	0.81[AMR][1000 genomes]
rs28751938	0.84[AMR][1000 genomes]
rs28793389	0.93[AMR][1000 genomes]
rs34396972	0.81[AMR][1000 genomes]
rs34942608	0.81[AMR][1000 genomes]
rs35830100	0.80[AMR][1000 genomes]
rs35933344	0.85[AMR][1000 genomes]
rs36028037	0.81[AMR][1000 genomes]
rs36080829	0.82[AMR][1000 genomes]
rs36108588	0.81[AMR][1000 genomes]
rs3898185	0.80[AMR][1000 genomes]
rs4284730	0.80[AMR][1000 genomes]
rs60519785	0.84[AMR][1000 genomes]
rs6535379	0.87[AMR][1000 genomes]
rs66517455	0.82[AMR][1000 genomes]
rs66783155	0.81[AMR][1000 genomes]
rs67558294	0.80[AMR][1000 genomes]
rs6820263	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6822133	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6828958	0.84[AMR][1000 genomes]
rs6850076	0.84[AMR][1000 genomes]
rs6855400	0.84[AMR][1000 genomes]
rs72647412	0.85[AMR][1000 genomes]
rs72860857	0.89[AMR][1000 genomes]
rs72860858	0.81[AMR][1000 genomes]
rs72862718	0.88[AMR][1000 genomes]
rs7661666	0.80[AMR][1000 genomes]
rs7669508	0.84[AMR][1000 genomes]
rs7672270	0.84[AMR][1000 genomes]
rs7677839	0.84[AMR][1000 genomes]
rs7684397	0.84[AMR][1000 genomes]
rs7686993	0.87[AMR][1000 genomes]
rs7690198	0.84[AMR][1000 genomes]
rs7695348	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7697608	0.84[AMR][1000 genomes]
rs949613	0.82[AMR][1000 genomes]
rs949614	0.82[AMR][1000 genomes]
rs955543	0.80[AMR][1000 genomes]
rs9994830	0.82[AMR][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	nsv1010552	chr4:76064415-76325430	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv998511	chr4:76184807-76398377	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2763368	chr4:76190070-76387413	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv461557	chr4:76212995-76363477	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv594688	chr4:76212995-76363477	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv879493	chr4:76264496-76332975	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv879494	chr4:76264496-76337998	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv594689	chr4:76309415-76323522	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island lncRNA	1 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	chr4:76312000-76317000	Weak transcription	Spleen	Spleen

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