Variant report

Variant	rs955634
Chromosome Location	chr10:116402786-116402787
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	chr10:116395685..116397875-chr10:116401409..116403061,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10444096	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10444097	0.89[ASN][1000 genomes]
rs10787539	0.91[JPT][hapmap]
rs10787540	0.90[JPT][hapmap]
rs11196798	0.90[JPT][hapmap]
rs11196802	0.90[JPT][hapmap]
rs11196804	0.85[ASN][1000 genomes]
rs11196806	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11196810	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11196813	0.89[ASN][1000 genomes]
rs11196814	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11196825	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11196826	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11196841	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11196844	0.82[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs11196845	0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs11196853	0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs11196854	0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11196856	0.92[ASN][1000 genomes]
rs11196858	0.92[ASN][1000 genomes]
rs11196859	0.91[ASN][1000 genomes]
rs11196861	0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs12146316	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12359503	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12360417	0.87[ASN][1000 genomes]
rs12763337	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12768716	0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12772864	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17719647	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34811081	0.89[ASN][1000 genomes]
rs4237504	0.89[ASN][1000 genomes]
rs4751620	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4752039	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4752040	0.87[ASN][1000 genomes]
rs4752044	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4752047	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4752071	0.86[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4752089	0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs7080854	0.90[JPT][hapmap]
rs7094673	0.90[JPT][hapmap]
rs7907371	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037308	chr10:116141946-116519765	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv540780	chr10:116141946-116519765	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv949138	chr10:116311531-116874477	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1038050	chr10:116315109-116895719	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv533027	chr10:116344641-116856352	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv3435429	chr10:116394152-117006347	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116393600-116405800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr10:116394400-116422600	Weak transcription	Fetal Intestine Small	intestine
3	chr10:116395800-116408400	Weak transcription	Psoas Muscle	Psoas
4	chr10:116396200-116404400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr10:116396200-116404600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr10:116396200-116408800	Weak transcription	Esophagus	oesophagus
7	chr10:116396600-116404600	Weak transcription	Pancreas	Pancrea
8	chr10:116397200-116409400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr10:116399200-116410400	Weak transcription	Brain Angular Gyrus	brain
10	chr10:116399400-116404200	Weak transcription	HUVEC	blood vessel
11	chr10:116399400-116404400	Weak transcription	NHEK	skin
12	chr10:116399400-116404600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:116399400-116404600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:116399400-116404600	Weak transcription	Right Atrium	heart
15	chr10:116399600-116402800	Weak transcription	Brain Anterior Caudate	brain
16	chr10:116399600-116404400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr10:116399600-116404800	Weak transcription	Fetal Lung	lung
18	chr10:116399600-116408600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr10:116399800-116403400	Weak transcription	Left Ventricle	heart
20	chr10:116399800-116404400	Weak transcription	A549	lung
21	chr10:116399800-116413800	Weak transcription	Spleen	Spleen
22	chr10:116400000-116406000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:116400200-116405600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:116400200-116408600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:116401000-116402800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr10:116401400-116403200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr10:116401800-116403400	Weak transcription	Lung	lung
28	chr10:116402000-116403000	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr10:116402000-116408400	Weak transcription	Right Ventricle	heart
30	chr10:116402600-116402800	Enhancers	HMEC	breast
31	chr10:116402600-116403000	Enhancers	Stomach Mucosa	stomach
32	chr10:116402600-116403200	Enhancers	Adipose Nuclei	Adipose
33	chr10:116402600-116403200	Enhancers	Fetal Heart	heart

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