Variant report

Variant	rs10214151
Chromosome Location	chr5:118778761-118778762
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10067734	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10069875	0.83[EUR][1000 genomes]
rs10072515	1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10078097	0.83[EUR][1000 genomes]
rs10478425	0.83[EUR][1000 genomes]
rs10478426	0.83[EUR][1000 genomes]
rs11241506	0.83[EUR][1000 genomes]
rs11948223	1.00[AMR][1000 genomes]
rs11951264	1.00[AMR][1000 genomes]
rs12656474	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12658566	0.83[EUR][1000 genomes]
rs13361193	0.83[EUR][1000 genomes]
rs2303003	0.83[EUR][1000 genomes]
rs3756512	0.83[EUR][1000 genomes]
rs58263192	0.83[EUR][1000 genomes]
rs58359191	1.00[AMR][1000 genomes]
rs61553637	1.00[AMR][1000 genomes]
rs73244920	0.95[AMR][1000 genomes]
rs73249951	0.83[EUR][1000 genomes]
rs7709833	0.95[AMR][1000 genomes]
rs7721314	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9327101	0.85[ASN][1000 genomes]
rs9327102	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030717	chr5:118709310-118836951	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv427732	chr5:118730999-119034741	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv4974	chr5:118750259-118795376	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1024455	chr5:118770429-119487982	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr5:118775400-118787600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr5:118775600-118781200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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