Variant report

Variant	rs11202897
Chromosome Location	chr10:90688847-90688848
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:90688740-90688937	K562	blood:	n/a	chr10:90688833-90688844
2	CEBPB	chr10:90688696-90688942	HepG2	liver:	n/a	chr10:90688833-90688844
3	CEBPB	chr10:90688712-90688986	A549	lung:	n/a	chr10:90688833-90688844

Variant related genes	Relation type
ACTA2-AS1	TF binding region

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1008719	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10887867	0.84[CEU][hapmap]
rs10887870	0.83[EUR][1000 genomes]
rs11202890	0.84[CEU][hapmap]
rs11202898	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11202899	1.00[CEU][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11202902	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11202906	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs11202907	0.91[CEU][hapmap]
rs11202908	0.90[YRI][hapmap]
rs11591231	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11595119	0.89[CEU][hapmap]
rs11596205	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1214564	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs12241401	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12241898	0.85[YRI][hapmap]
rs12248284	0.84[CEU][hapmap]
rs12254084	0.91[CEU][hapmap]
rs12254856	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12267680	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17114152	0.84[CEU][hapmap]
rs17114327	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs2119685	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs2439707	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs2481918	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs41284106	0.96[EUR][1000 genomes]
rs41317244	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4431933	0.84[CEU][hapmap]
rs45493098	0.96[EUR][1000 genomes]
rs56104559	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56228317	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56268252	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57807025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs59737591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66478243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7078383	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs7085698	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs7090631	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs7098235	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs72809310	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72809311	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72809314	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72809318	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72809335	0.98[EUR][1000 genomes]
rs72809337	0.96[EUR][1000 genomes]
rs72809342	0.96[EUR][1000 genomes]
rs7897521	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs7915393	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs988584	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv831942	chr10:90564697-90730352	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv831943	chr10:90664836-90865834	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90655200-90701400	Weak transcription	Gastric	stomach
2	chr10:90659600-90689800	Weak transcription	Esophagus	oesophagus
3	chr10:90660400-90695000	Weak transcription	Fetal Brain Male	brain
4	chr10:90661600-90692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:90664200-90694600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr10:90664400-90691200	Weak transcription	Small Intestine	intestine
7	chr10:90664400-90694800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:90666000-90692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:90668400-90694800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr10:90669800-90689200	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr10:90675800-90696400	Weak transcription	Spleen	Spleen
12	chr10:90678000-90694800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr10:90680800-90689200	Strong transcription	Primary T cells from cord blood	blood
14	chr10:90681400-90697800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:90682000-90694800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr10:90683400-90692000	Weak transcription	Hela-S3	cervix
17	chr10:90683600-90692200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr10:90683800-90694800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr10:90684600-90692200	Weak transcription	Colonic Mucosa	Colon
20	chr10:90684800-90694800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr10:90685000-90692000	Weak transcription	NHEK	skin
22	chr10:90685600-90689400	Strong transcription	Primary hematopoietic stem cells	blood
23	chr10:90685600-90691800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr10:90685800-90692200	Weak transcription	Fetal Intestine Small	intestine
25	chr10:90685800-90695000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr10:90686000-90694800	Weak transcription	Stomach Mucosa	stomach
27	chr10:90686000-90697600	Weak transcription	Left Ventricle	heart
28	chr10:90686200-90694600	Weak transcription	Fetal Kidney	kidney
29	chr10:90686600-90692200	Weak transcription	NH-A	brain
30	chr10:90686600-90694800	Weak transcription	Brain Substantia Nigra	brain
31	chr10:90686800-90694800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr10:90686800-90694800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr10:90686800-90694800	Weak transcription	Liver	Liver
34	chr10:90686800-90697800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr10:90687000-90692200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr10:90687000-90692200	Weak transcription	Brain Anterior Caudate	brain
37	chr10:90687000-90692200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:90687000-90695000	Weak transcription	Primary B cells from cord blood	blood
39	chr10:90687200-90689400	Strong transcription	HSMM	muscle
40	chr10:90687200-90692200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr10:90687200-90692200	Weak transcription	Brain Hippocampus Middle	brain
42	chr10:90687400-90692200	Weak transcription	Brain Angular Gyrus	brain
43	chr10:90687400-90692200	Weak transcription	Brain Cingulate Gyrus	brain
44	chr10:90687400-90692200	Weak transcription	A549	lung
45	chr10:90687400-90693400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:90687400-90694600	Weak transcription	HSMMtube	muscle
47	chr10:90687400-90694800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:90687400-90695000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr10:90687600-90691000	Weak transcription	Colon Smooth Muscle	Colon
50	chr10:90687600-90691200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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