Variant report

Variant	rs9490136
Chromosome Location	chr6:121523736-121523737
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10428866	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11154003	0.89[ASN][1000 genomes]
rs1273711	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs1273719	1.00[CEU][hapmap]
rs1273749	1.00[GIH][hapmap]
rs1273754	1.00[GIH][hapmap];0.82[MEX][hapmap]
rs1273765	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1273773	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1273777	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1343072	0.89[ASN][1000 genomes]
rs1604279	0.89[ASN][1000 genomes]
rs17083186	1.00[CEU][hapmap]
rs17083373	1.00[CEU][hapmap]
rs17083415	1.00[CEU][hapmap]
rs17154	1.00[CEU][hapmap]
rs1776810	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1827299	0.89[ASN][1000 genomes]
rs2102102	0.86[ASN][1000 genomes]
rs2133991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2133992	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs2892765	1.00[CEU][hapmap]
rs2892766	0.83[ASN][1000 genomes]
rs35583988	0.89[ASN][1000 genomes]
rs4072142	1.00[CEU][hapmap]
rs4368847	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4371872	1.00[CEU][hapmap]
rs4476866	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs4610600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4946547	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs4946562	0.85[CHB][hapmap]
rs4946563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58729190	0.97[ASN][1000 genomes]
rs6569180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6903467	1.00[CEU][hapmap]
rs6936507	0.86[ASN][1000 genomes]
rs7450022	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs7451033	1.00[CEU][hapmap]
rs7741356	1.00[CEU][hapmap]
rs7742071	1.00[CEU][hapmap]
rs7743455	1.00[CEU][hapmap]
rs7744891	0.82[CEU][hapmap]
rs7749984	1.00[CEU][hapmap]
rs7761551	1.00[CEU][hapmap]
rs7765795	1.00[CEU][hapmap]
rs7767455	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.97[ASN][1000 genomes]
rs785400	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs785407	1.00[CEU][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs905024	0.92[CHB][hapmap];0.88[ASN][1000 genomes]
rs905025	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs924528	0.87[ASN][1000 genomes]
rs9320793	0.89[ASN][1000 genomes]
rs9320794	0.92[CHB][hapmap];0.85[CHD][hapmap];0.89[ASN][1000 genomes]
rs9320802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.97[ASN][1000 genomes]
rs9372640	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs9372641	0.89[ASN][1000 genomes]
rs9372643	0.89[ASN][1000 genomes]
rs9372644	0.89[ASN][1000 genomes]
rs9372646	0.90[CHB][hapmap]
rs9372647	0.86[ASN][1000 genomes]
rs9375007	0.86[ASN][1000 genomes]
rs9375008	0.86[ASN][1000 genomes]
rs9375009	0.89[ASN][1000 genomes]
rs9375011	0.92[CHB][hapmap];0.85[CHD][hapmap];0.86[ASN][1000 genomes]
rs9375012	0.92[CHB][hapmap];0.86[ASN][1000 genomes]
rs9387926	1.00[CEU][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs9387928	0.89[ASN][1000 genomes]
rs9387930	0.86[ASN][1000 genomes]
rs9398623	0.92[CHB][hapmap];0.85[CHD][hapmap];0.89[ASN][1000 genomes]
rs9398625	0.92[CHB][hapmap];0.86[ASN][1000 genomes]
rs9398631	0.85[CHB][hapmap];0.82[CHD][hapmap]
rs9401373	0.89[ASN][1000 genomes]
rs9401374	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs9401375	0.92[CHB][hapmap];0.88[ASN][1000 genomes]
rs9401376	0.89[ASN][1000 genomes]
rs9401377	0.89[ASN][1000 genomes]
rs9401378	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs9401379	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs9490149	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023384	chr6:121235867-121683448	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv530527	chr6:121298528-121789855	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv604572	chr6:121465011-121544876	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv11992	chr6:121519481-121526100	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
5	nsv514384	chr6:121521453-121524581	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv1821620	chr6:121521902-121524055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	nsv442006	chr6:121521902-121524055	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv2760998	chr6:121521906-121524055	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv517605	chr6:121523736-121524231	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv524172	chr6:121523736-121526898	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121478800-121535400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:121480200-121535600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr6:121480800-121535400	Weak transcription	Fetal Intestine Large	intestine
4	chr6:121481000-121535400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:121487400-121556000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:121495200-121529400	Weak transcription	Primary B cells from cord blood	blood
7	chr6:121496800-121535400	Weak transcription	Fetal Lung	lung
8	chr6:121498600-121535400	Weak transcription	Pancreas	Pancrea
9	chr6:121499800-121535800	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:121500000-121529000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:121502600-121529000	Weak transcription	Left Ventricle	heart
12	chr6:121509600-121575400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:121511400-121535400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:121511800-121535400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:121514200-121535600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:121514600-121529400	Weak transcription	Ovary	ovary
17	chr6:121515000-121535800	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr6:121515200-121535400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:121515200-121535400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr6:121515400-121535400	Weak transcription	Gastric	stomach
21	chr6:121515600-121544200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:121515800-121532800	Weak transcription	Fetal Intestine Small	intestine
23	chr6:121516000-121535400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr6:121516000-121560200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr6:121516800-121535400	Weak transcription	Esophagus	oesophagus
26	chr6:121517400-121524000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr6:121517800-121535400	Weak transcription	Aorta	Aorta
28	chr6:121518000-121529000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:121518200-121535400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr6:121518600-121535400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr6:121519000-121531800	Weak transcription	Primary T cells from cord blood	blood
32	chr6:121519000-121535600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr6:121519200-121525600	Weak transcription	Dnd41	blood
34	chr6:121520200-121535400	Weak transcription	Adipose Nuclei	Adipose
35	chr6:121521000-121535400	Weak transcription	Brain Anterior Caudate	brain
36	chr6:121522600-121533000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:121522600-121535400	Weak transcription	Primary hematopoietic stem cells	blood

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