Variant report

Variant	rs35882323
Chromosome Location	chr11:33635261-33635262
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10768008	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10836077	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10836078	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11032300	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11032305	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11032306	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11032307	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11032309	0.82[EUR][1000 genomes]
rs11032310	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11032311	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11032317	0.86[EUR][1000 genomes]
rs11823713	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12277742	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12806278	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1321013	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16924469	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2076625	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2076626	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2273115	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2273117	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2901321	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34316641	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34418271	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34862267	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34960900	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35112514	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35867834	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35917507	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4755201	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4755207	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4755718	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55891606	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61888295	0.82[EUR][1000 genomes]
rs61888322	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6484658	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7102647	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7109146	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7110105	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7119677	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7122768	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7123643	0.87[EUR][1000 genomes]
rs7128963	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs735327	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7939586	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7945168	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044478	chr11:33008435-33656273	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised 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	65 gene(s)	inside rSNPs	diseases
2	nsv1050944	chr11:33043155-33656273	Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv540993	chr11:33043155-33656273	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv529212	chr11:33053073-33641691	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	nsv869418	chr11:33053073-33662479	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
6	nsv1041680	chr11:33249367-33637249	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv540997	chr11:33249367-33637249	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv832112	chr11:33469782-33683052	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv832113	chr11:33609202-33767781	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 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	chr11:33594600-33644000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:33605800-33642400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:33606600-33642000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:33615800-33635400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:33619400-33639000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:33620200-33640200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr11:33620800-33639200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:33621400-33637400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr11:33627200-33643400	Weak transcription	HSMMtube	muscle
10	chr11:33628800-33635400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:33628800-33642400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:33630000-33641600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr11:33632200-33638000	Weak transcription	NH-A	brain
14	chr11:33632800-33635400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:33632800-33638200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:33632800-33638800	Weak transcription	Brain Germinal Matrix	brain
17	chr11:33632800-33639000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:33632800-33642400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:33633800-33635400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:33633800-33652400	Weak transcription	Fetal Brain Female	brain
21	chr11:33634600-33643800	Weak transcription	HUVEC	blood vessel
22	chr11:33635000-33636000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:33635000-33638600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:33635000-33644800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:33635200-33638400	Enhancers	HMEC	breast

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