Variant report

Variant	rs7841921
Chromosome Location	chr8:10212969-10212970
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10087341	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10096337	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10105867	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10283145	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11774221	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11777976	0.82[JPT][hapmap]
rs11990519	0.82[JPT][hapmap]
rs13252982	0.82[JPT][hapmap]
rs13254263	0.82[JPT][hapmap]
rs17151843	0.89[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17151854	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.85[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17151859	1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs17708276	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs17709397	1.00[JPT][hapmap]
rs17765901	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs17767019	0.94[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs1986676	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2001364	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28402777	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28406568	0.82[ASN][1000 genomes]
rs28491054	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2952185	1.00[CHD][hapmap]
rs2975680	1.00[CHB][hapmap]
rs2975682	1.00[CHB][hapmap]
rs3750310	0.82[JPT][hapmap]
rs3812495	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4074083	0.82[JPT][hapmap]
rs4342552	0.82[JPT][hapmap]
rs4433149	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4526367	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs4610752	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4840480	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4841352	0.82[JPT][hapmap]
rs6601443	1.00[CHD][hapmap]
rs6601451	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs68071218	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6984111	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6989657	0.82[JPT][hapmap]
rs73197263	0.92[EUR][1000 genomes]
rs7813873	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7824675	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7831557	0.82[JPT][hapmap]
rs7833781	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv1016347	chr8:10091475-10223667	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	nsv1018940	chr8:10200886-10220973	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10192600-10282400	Weak transcription	Gastric	stomach
2	chr8:10193000-10215400	Weak transcription	Fetal Intestine Small	intestine
3	chr8:10193000-10235000	Weak transcription	Pancreas	Pancrea
4	chr8:10193600-10220400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr8:10196800-10214200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:10196800-10228000	Weak transcription	Liver	Liver
7	chr8:10201800-10221800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:10204000-10219800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:10204400-10221800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:10206000-10213600	Enhancers	Fetal Brain Male	brain
11	chr8:10206200-10222800	Weak transcription	Aorta	Aorta
12	chr8:10206800-10214600	Enhancers	Fetal Thymus	thymus
13	chr8:10208000-10213000	Weak transcription	Spleen	Spleen
14	chr8:10208400-10218200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr8:10208800-10220400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:10209200-10213600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr8:10209400-10220600	Weak transcription	Brain Angular Gyrus	brain
18	chr8:10209600-10213600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:10210600-10218400	Weak transcription	Left Ventricle	heart
20	chr8:10210600-10220200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr8:10211000-10214000	Enhancers	Primary T cells from cord blood	blood
22	chr8:10211000-10215400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr8:10211200-10213000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:10211200-10220000	Weak transcription	Right Atrium	heart
25	chr8:10211400-10213000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr8:10211800-10214000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:10211800-10214000	Weak transcription	Fetal Brain Female	brain
28	chr8:10211800-10214600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr8:10212000-10213200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr8:10212000-10213800	Weak transcription	Thymus	Thymus
31	chr8:10212800-10213600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr8:10212800-10214200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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