Variant report

Variant	rs11226134
Chromosome Location	chr11:103931025-103931026
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10736631	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10895570	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226128	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11226132	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11226139	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226146	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11226150	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12792763	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34103966	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34739592	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35982603	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs615290	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61892152	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs681959	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv948974	chr11:103082558-103932207	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv2760322	chr11:103760085-104374141	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1051448	chr11:103864766-104274112	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv541157	chr11:103864766-104274112	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1043976	chr11:103881236-104526403	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:103921400-103932400	Weak transcription	Aorta	Aorta
2	chr11:103925000-103931600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr11:103926000-103934400	Weak transcription	Ovary	ovary
4	chr11:103928400-103939400	Weak transcription	Pancreas	Pancrea
5	chr11:103930400-103934200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:103930400-103934200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr11:103930600-103931200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:103930600-103931400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:103930600-103931400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr11:103930600-103931400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:103930600-103931600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:103930800-103931200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:103930800-103931200	Enhancers	Adipose Nuclei	Adipose
14	chr11:103930800-103931400	Enhancers	HMEC	breast
15	chr11:103930800-103931800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:103930800-103936000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr11:103931000-103931200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:103931000-103931200	Enhancers	Left Ventricle	heart
19	chr11:103931000-103931200	Enhancers	Right Atrium	heart
20	chr11:103931000-103931400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:103931000-103931400	Enhancers	Brain Germinal Matrix	brain
22	chr11:103931000-103931600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr11:103931000-103932200	Enhancers	Fetal Brain Female	brain
24	chr11:103931000-103932400	Enhancers	Fetal Brain Male	brain
25	chr11:103931000-103932800	Enhancers	Monocytes-CD14+_RO01746	blood

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