Variant report

Variant	rs6687405
Chromosome Location	chr1:158240757-158240758
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10797006	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10908644	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10908645	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11264949	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11264950	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11264952	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11486132	0.81[EUR][1000 genomes]
rs11488686	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12027881	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12077077	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12077284	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12089293	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12089433	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12095313	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12407446	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12409817	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12751238	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1813777	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1923141	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs366316	0.86[EUR][1000 genomes]
rs378137	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs389293	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs440710	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6685958	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7539343	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv508626	chr1:158161932-158242158	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv831692	chr1:158223459-158392016	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr1:158228800-158243600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:158237400-158242800	Weak transcription	Fetal Thymus	thymus
3	chr1:158240600-158242600	Enhancers	Dnd41	blood

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