Variant report

Variant	rs11042913
Chromosome Location	chr11:10686561-10686562
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:10662540..10664082-chr11:10686222..10688544,2	K562	blood:
2	chr11:10686058..10688524-chr11:10689302..10691752,2	MCF-7	breast:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10219376	0.82[EUR][1000 genomes]
rs10431031	0.86[EUR][1000 genomes]
rs10770128	0.95[CEU][hapmap];0.91[EUR][1000 genomes]
rs10770129	0.95[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10770130	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10770132	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs10770133	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs10840451	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs10840454	0.93[EUR][1000 genomes]
rs10840455	0.90[CEU][hapmap];0.93[EUR][1000 genomes]
rs10840456	0.95[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10840458	0.87[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10840459	0.89[ASN][1000 genomes]
rs10840460	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840461	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840462	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840463	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840464	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840465	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840466	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840467	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10840468	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs11042909	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11042910	0.85[JPT][hapmap]
rs11042911	0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12363422	0.85[ASN][1000 genomes]
rs12420672	0.85[ASN][1000 genomes]
rs12420675	0.85[ASN][1000 genomes]
rs1390572	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1390573	0.87[ASN][1000 genomes]
rs1425149	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425150	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425151	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1544862	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1544863	0.87[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs16908157	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs16908159	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs16908162	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1845832	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1874444	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1895712	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2098840	0.95[ASN][1000 genomes]
rs34554801	0.89[ASN][1000 genomes]
rs35040034	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35165550	0.85[ASN][1000 genomes]
rs4243916	0.87[ASN][1000 genomes]
rs4909946	0.87[ASN][1000 genomes]
rs4910166	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7123106	0.81[EUR][1000 genomes]
rs7127014	0.83[EUR][1000 genomes]
rs722274	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs745336	0.87[ASN][1000 genomes]
rs750540	0.85[ASN][1000 genomes]
rs7925193	0.90[JPT][hapmap]
rs7933525	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7935285	0.94[CEU][hapmap];0.95[EUR][1000 genomes]
rs7938027	0.87[ASN][1000 genomes]
rs7938635	0.90[CEU][hapmap];0.95[EUR][1000 genomes]
rs7939662	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7939686	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs881870	0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs903825	0.85[ASN][1000 genomes]
rs903826	0.85[ASN][1000 genomes]
rs903827	0.85[ASN][1000 genomes]
rs903828	0.85[ASN][1000 genomes]
rs9633862	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9633863	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430319	chr11:10027543-10711224	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv832063	chr11:10618485-10785281	ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10674600-10689600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:10680600-10696200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:10680800-10687200	Weak transcription	Small Intestine	intestine
4	chr11:10681000-10687800	Weak transcription	Brain Angular Gyrus	brain
5	chr11:10681000-10688800	Weak transcription	Colonic Mucosa	Colon
6	chr11:10681600-10689000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr11:10682200-10687400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr11:10682200-10688200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:10682200-10690400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr11:10682400-10687600	Weak transcription	Osteobl	bone
11	chr11:10682600-10687800	Weak transcription	A549	lung
12	chr11:10682600-10687800	Weak transcription	Hela-S3	cervix
13	chr11:10682600-10688800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:10682800-10688200	Weak transcription	Right Atrium	heart
15	chr11:10683000-10687800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr11:10683200-10687400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:10683400-10687600	Strong transcription	Fetal Stomach	stomach
18	chr11:10683400-10687800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:10683600-10687400	Weak transcription	NHLF	lung
20	chr11:10683800-10692400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:10684200-10687400	Enhancers	Left Ventricle	heart
22	chr11:10684200-10687600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr11:10684400-10692000	Enhancers	Ovary	ovary
24	chr11:10684800-10689200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr11:10685000-10687600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:10685000-10688400	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr11:10685000-10689200	Enhancers	Brain Anterior Caudate	brain
28	chr11:10685000-10690800	Enhancers	NHDF-Ad	bronchial
29	chr11:10685600-10686600	Enhancers	Brain Cingulate Gyrus	brain
30	chr11:10685800-10686800	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr11:10685800-10687400	Genic enhancers	Aorta	Aorta
32	chr11:10685800-10688000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr11:10685800-10688200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr11:10686000-10686600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:10686000-10687400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:10686000-10688200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr11:10686000-10688800	Weak transcription	Esophagus	oesophagus
38	chr11:10686000-10690400	Weak transcription	Spleen	Spleen
39	chr11:10686000-10692200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr11:10686200-10687200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr11:10686200-10687200	Weak transcription	Lung	lung
42	chr11:10686200-10687800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:10686200-10688200	Weak transcription	Adipose Nuclei	Adipose
44	chr11:10686200-10688200	Weak transcription	Brain Substantia Nigra	brain
45	chr11:10686200-10688200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr11:10686200-10688800	Weak transcription	Psoas Muscle	Psoas
47	chr11:10686200-10690400	Weak transcription	Fetal Intestine Small	intestine
48	chr11:10686200-10690400	Weak transcription	Placenta	Placenta
49	chr11:10686400-10686800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:10686400-10686800	Genic enhancers	Stomach Smooth Muscle	stomach

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