Variant report

Variant	rs4413770
Chromosome Location	chr8:63838803-63838804
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:63834445..63836856-chr8:63836928..63839834,2	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10090886	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10093212	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10100456	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10106324	1.00[CHB][hapmap]
rs10808728	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10957253	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11992351	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12335094	0.89[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs12679222	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13272238	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1378522	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1378523	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1455574	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17273584	0.86[EUR][1000 genomes]
rs1869729	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1869730	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1869731	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1869732	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2353388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35185274	0.86[EUR][1000 genomes]
rs35478421	0.86[EUR][1000 genomes]
rs35583011	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4237056	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4237058	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4237059	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4237060	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4237061	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4276687	0.86[EUR][1000 genomes]
rs4279586	0.88[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs4284039	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4292679	0.86[EUR][1000 genomes]
rs4352845	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4360287	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4368971	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4374987	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4376492	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4377959	0.84[EUR][1000 genomes]
rs4397399	0.85[EUR][1000 genomes]
rs4400383	0.85[EUR][1000 genomes]
rs4412364	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4434615	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4446729	1.00[CHB][hapmap]
rs4466391	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4478566	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4504631	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4509316	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4521749	0.86[EUR][1000 genomes]
rs4573266	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4593533	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4626587	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4739021	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5007413	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs6998134	1.00[CHB][hapmap]
rs6998501	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6999604	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7000012	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7000020	0.86[EUR][1000 genomes]
rs7003413	1.00[CHB][hapmap]
rs7010484	0.89[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs7387326	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7388305	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs7463670	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7830289	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7839216	0.83[EUR][1000 genomes]
rs7839874	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831341	chr8:63658694-63852213	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63836200-63839200	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:63838600-63839000	Weak transcription	Fetal Kidney	kidney
3	chr8:63838600-63841400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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