Variant report

Variant	rs1390281
Chromosome Location	chr4:90512099-90512100
allele	C/T
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:21)

rs_ID	r²[population]
rs10031817	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1036084	0.95[ASN][1000 genomes]
rs11097227	0.99[ASN][1000 genomes]
rs12108375	1.00[ASN][1000 genomes]
rs12507346	1.00[ASN][1000 genomes]
rs1495549	1.00[ASN][1000 genomes]
rs1603250	1.00[ASN][1000 genomes]
rs17015858	0.86[CEU][hapmap];0.81[CHB][hapmap];0.80[JPT][hapmap]
rs17015996	0.82[ASN][1000 genomes]
rs28545331	0.83[ASN][1000 genomes]
rs28673968	0.82[ASN][1000 genomes]
rs28881549	0.82[ASN][1000 genomes]
rs3733449	0.82[ASN][1000 genomes]
rs58310666	0.94[ASN][1000 genomes]
rs61648356	0.94[ASN][1000 genomes]
rs6835887	0.81[ASN][1000 genomes]
rs6842271	0.87[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6855067	0.95[ASN][1000 genomes]
rs72655897	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7683607	0.95[ASN][1000 genomes]
rs9985612	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv830003	chr4:90331829-90538134	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv879534	chr4:90498133-90591889	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90511400-90512400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:90511800-90512600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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