Variant report

Variant	rs4355737
Chromosome Location	chr8:95827173-95827174
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:95826436..95828535-chr8:95832884..95835049,2	K562	blood:
2	chr8:95825181..95829614-chr8:95834341..95841614,7	MCF-7	breast:
3	chr8:95731513..95733267-chr8:95825138..95827545,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164941	Chromatin interaction
ENSG00000156162	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10956927	0.94[CEU][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11774806	0.97[ASN][1000 genomes]
rs11775475	0.84[CEU][hapmap];0.91[EUR][1000 genomes]
rs11775899	0.82[EUR][1000 genomes]
rs11776131	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11776489	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11776687	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11777132	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11777353	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11778250	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11779041	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11779252	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11781099	0.97[ASN][1000 genomes]
rs11781188	0.93[ASN][1000 genomes]
rs11781429	0.95[CEU][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11781712	0.96[EUR][1000 genomes]
rs11781843	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11782617	0.94[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11783522	0.84[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11783589	0.95[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11784299	0.94[CEU][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11786021	0.97[ASN][1000 genomes]
rs11786088	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11786389	0.95[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11786429	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11786451	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11787377	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11787442	0.97[ASN][1000 genomes]
rs12056517	0.95[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12056808	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16893774	0.84[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16917079	0.94[CEU][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16917081	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16917082	0.94[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16917093	0.95[CEU][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16917102	0.81[EUR][1000 genomes]
rs16917117	0.82[EUR][1000 genomes]
rs17359493	0.95[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28399553	0.84[EUR][1000 genomes]
rs28399563	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28399571	0.89[EUR][1000 genomes]
rs4073916	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4075834	1.00[CEU][hapmap];0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4345531	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57063661	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57773845	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58489999	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58675831	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59091366	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59265059	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59521030	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60171840	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6986418	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6989591	0.94[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7009940	0.80[EUR][1000 genomes]
rs73269162	0.97[ASN][1000 genomes]
rs73269170	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73269188	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73269191	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73269198	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73269199	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73271148	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73271178	0.84[EUR][1000 genomes]
rs7834966	0.89[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription 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 miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4355737	INTS8	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95825600-95827800	Enhancers	Fetal Intestine Large	intestine
2	chr8:95825800-95827200	Weak transcription	Stomach Mucosa	stomach
3	chr8:95826800-95827200	Flanking Active TSS	A549	lung
4	chr8:95826800-95827400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr8:95826800-95827400	Flanking Active TSS	HepG2	liver
6	chr8:95826800-95827600	Enhancers	Duodenum Mucosa	Duodenum
7	chr8:95826800-95827600	Active TSS	Rectal Mucosa Donor 29	rectum

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