Variant report

Variant	rs7822092
Chromosome Location	chr8:10246123-10246124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10240370..10243141-chr8:10246115..10249322,3	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10094308	1.00[YRI][hapmap]
rs11249998	0.83[AFR][1000 genomes]
rs11250000	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4841332	1.00[YRI][hapmap]
rs4841340	1.00[AFR][1000 genomes]
rs4841347	1.00[AFR][1000 genomes]
rs6601460	1.00[AFR][1000 genomes]
rs6989054	1.00[YRI][hapmap]
rs7463129	1.00[YRI][hapmap]
rs7819111	1.00[AFR][1000 genomes]
rs7820897	1.00[YRI][hapmap]
rs7842777	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 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

No data

Chromatin state (count:23 , 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	chr8:10228600-10247800	Weak transcription	Liver	Liver
4	chr8:10233800-10252400	Weak transcription	Fetal Brain Male	brain
5	chr8:10235200-10252400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:10236200-10247400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr8:10236200-10252600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
10	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
11	chr8:10237200-10247400	Weak transcription	Lung	lung
12	chr8:10240400-10256000	Weak transcription	Adipose Nuclei	Adipose
13	chr8:10240400-10256800	Weak transcription	Left Ventricle	heart
14	chr8:10241200-10247400	Weak transcription	Spleen	Spleen
15	chr8:10241800-10246800	Weak transcription	Primary T cells from cord blood	blood
16	chr8:10241800-10249600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr8:10242000-10246200	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:10242000-10255800	Weak transcription	Brain Germinal Matrix	brain
19	chr8:10242200-10248200	Weak transcription	Fetal Brain Female	brain
20	chr8:10243000-10246200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:10244800-10251200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:10245000-10247400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr8:10245000-10253400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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