Variant report

Variant	rs7840461
Chromosome Location	chr8:10255356-10255357
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11249999	0.80[ASN][1000 genomes]
rs11250001	0.81[CHB][hapmap];0.86[ASN][1000 genomes]
rs11250002	0.81[CHB][hapmap];0.84[ASN][1000 genomes]
rs11250006	0.80[ASN][1000 genomes]
rs11783514	0.94[CHB][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11989029	0.82[AMR][1000 genomes]
rs11989640	0.81[CHB][hapmap];0.84[ASN][1000 genomes]
rs12541491	0.81[CHB][hapmap];0.83[ASN][1000 genomes]
rs12544727	0.81[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13254942	0.81[CHB][hapmap];0.83[ASN][1000 genomes]
rs13264580	0.80[ASN][1000 genomes]
rs13273009	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs17151892	0.88[CHB][hapmap];0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17151898	0.88[CHB][hapmap];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17151899	0.80[CHB][hapmap];0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17151903	0.87[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1986677	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs2001337	0.80[ASN][1000 genomes]
rs2001338	0.80[ASN][1000 genomes]
rs2001365	0.88[CHB][hapmap];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6601447	0.87[CHB][hapmap]
rs6985267	0.94[JPT][hapmap]
rs7821526	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7842443	0.80[CHB][hapmap];0.82[JPT][hapmap]
rs9650650	0.80[ASN][1000 genomes]
rs9657538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9657539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv890347	chr8:10153082-10331636	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv527326	chr8:10199548-10320019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv465460	chr8:10241411-10290566	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
9	nsv610265	chr8:10241411-10290566	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv610266	chr8:10250758-10294330	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	nsv1019701	chr8:10254709-10279269	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10192600-10282400	Weak transcription	Gastric	stomach
2	chr8:10224000-10255800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
5	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
6	chr8:10240400-10256000	Weak transcription	Adipose Nuclei	Adipose
7	chr8:10240400-10256800	Weak transcription	Left Ventricle	heart
8	chr8:10242000-10255800	Weak transcription	Brain Germinal Matrix	brain
9	chr8:10249000-10258200	Enhancers	Fetal Muscle Leg	muscle
10	chr8:10249000-10275200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:10250000-10255400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:10252000-10258200	Enhancers	Fetal Muscle Trunk	muscle
13	chr8:10252400-10257200	Enhancers	HepG2	liver
14	chr8:10252800-10255800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:10253000-10255800	Weak transcription	HSMM	muscle
16	chr8:10253600-10255800	Weak transcription	Brain Hippocampus Middle	brain
17	chr8:10253600-10255800	Weak transcription	Right Atrium	heart
18	chr8:10253800-10255400	Weak transcription	Brain Anterior Caudate	brain
19	chr8:10253800-10256000	Weak transcription	Fetal Brain Male	brain
20	chr8:10253800-10257800	Weak transcription	Spleen	Spleen
21	chr8:10254000-10255600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:10254200-10261200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr8:10254400-10257400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:10254800-10256000	Enhancers	Brain Angular Gyrus	brain
25	chr8:10254800-10257000	Enhancers	Liver	Liver
26	chr8:10255000-10257000	Enhancers	Brain Cingulate Gyrus	brain
27	chr8:10255200-10255600	Weak transcription	Fetal Brain Female	brain
28	chr8:10255200-10255800	Weak transcription	HSMMtube	muscle
29	chr8:10255200-10267800	Weak transcription	Primary T cells from cord blood	blood

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