Variant report

Variant	rs10276533
Chromosome Location	chr7:117241859-117241860
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10266116	1.00[JPT][hapmap]
rs1042180	1.00[JPT][hapmap]
rs11974545	0.94[CEU][hapmap];0.95[EUR][1000 genomes]
rs12534233	0.91[EUR][1000 genomes]
rs1429568	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs17140297	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs17549557	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs17550567	0.81[CEU][hapmap]
rs1800136	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs2079178	0.81[CEU][hapmap]
rs213979	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213980	0.94[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs213981	0.94[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs213986	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs213988	0.94[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs213989	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs214163	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs214164	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2188150	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2213958	1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2518879	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35050470	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35216437	0.91[EUR][1000 genomes]
rs35244428	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4727855	0.80[CEU][hapmap]
rs6980032	1.00[JPT][hapmap]
rs739797	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889078	chr7:117135025-117246315	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv889082	chr7:117203417-117246315	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv889083	chr7:117203417-117256374	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv889084	chr7:117212723-117246315	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv889085	chr7:117214089-117246315	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv889086	chr7:117214089-117252873	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv889087	chr7:117226766-117246315	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv981820	chr7:117239985-117242827	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117233000-117245000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr7:117236200-117243400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr7:117236200-117244800	Weak transcription	Pancreas	Pancrea
4	chr7:117236200-117245600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:117236600-117245600	Weak transcription	Colonic Mucosa	Colon
6	chr7:117236800-117244800	Weak transcription	Fetal Intestine Large	intestine
7	chr7:117237600-117245000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr7:117238200-117242000	Weak transcription	Fetal Intestine Small	intestine
9	chr7:117238200-117243600	Weak transcription	Fetal Thymus	thymus
10	chr7:117238200-117243600	Weak transcription	Dnd41	blood
11	chr7:117240600-117244800	Weak transcription	A549	lung
12	chr7:117241600-117242200	Enhancers	HUVEC	blood vessel

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