Variant report

Variant	rs1351736
Chromosome Location	chr11:104026977-104026978
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	chr11:104021400..104024354-chr11:104024715..104027620,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10502026	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs10502027	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs10502028	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs10502029	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs10895576	0.80[EUR][1000 genomes]
rs10895577	0.80[EUR][1000 genomes]
rs10895580	0.82[EUR][1000 genomes]
rs10895584	1.00[CEU][hapmap]
rs10895585	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs11226185	1.00[CEU][hapmap];0.81[MEX][hapmap];0.80[EUR][1000 genomes]
rs11226186	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs11226189	0.80[EUR][1000 genomes]
rs11226193	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs11226194	0.82[EUR][1000 genomes]
rs11226195	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs11226196	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs11226197	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs11226198	0.82[EUR][1000 genomes]
rs11226199	0.82[EUR][1000 genomes]
rs11226200	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12224797	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12224814	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12226274	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12273661	1.00[CEU][hapmap];0.81[MEX][hapmap];0.80[EUR][1000 genomes]
rs12277818	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12279801	1.00[CEU][hapmap];0.81[MEX][hapmap];0.80[EUR][1000 genomes]
rs12280073	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12281544	0.82[EUR][1000 genomes]
rs12284612	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12284794	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs12285176	0.82[EUR][1000 genomes]
rs12286104	0.82[EUR][1000 genomes]
rs12290767	0.82[EUR][1000 genomes]
rs1351735	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1483519	1.00[CEU][hapmap]
rs1501456	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1501457	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs1532674	0.82[EUR][1000 genomes]
rs17093712	0.82[EUR][1000 genomes]
rs17101978	1.00[CEU][hapmap];0.81[MEX][hapmap];0.80[EUR][1000 genomes]
rs17102032	0.82[EUR][1000 genomes]
rs17102035	0.82[EUR][1000 genomes]
rs17102040	0.82[EUR][1000 genomes]
rs17102052	0.82[EUR][1000 genomes]
rs17102060	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17102089	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17102103	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1969076	0.82[EUR][1000 genomes]
rs361292	1.00[CEU][hapmap];0.90[MEX][hapmap]
rs4403779	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755008	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs4755009	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7395216	0.82[EUR][1000 genomes]
rs7396344	0.82[EUR][1000 genomes]
rs7396395	0.82[EUR][1000 genomes]
rs7396472	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs924560	0.82[EUR][1000 genomes]
rs924561	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[EUR][1000 genomes]
rs924562	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	nsv1040367	chr11:103956747-104440470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
6	esv1834487	chr11:103959760-104026977	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv430426	chr11:103978540-104099790	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104005800-104031000	Weak transcription	Aorta	Aorta
2	chr11:104013600-104033600	Weak transcription	Left Ventricle	heart
3	chr11:104013800-104033600	Weak transcription	Pancreas	Pancrea
4	chr11:104017400-104027800	Weak transcription	Ovary	ovary
5	chr11:104019600-104032200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:104024400-104028000	Weak transcription	Fetal Stomach	stomach
7	chr11:104024400-104032800	Weak transcription	A549	lung
8	chr11:104024600-104033400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr11:104025200-104030400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:104025400-104032200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr11:104025400-104033000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:104025400-104033600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:104025600-104032800	Weak transcription	Fetal Brain Female	brain
14	chr11:104025600-104033400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:104026200-104027400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:104026200-104029000	Enhancers	Brain Germinal Matrix	brain
17	chr11:104026400-104033400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr11:104026600-104028200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:104026600-104030400	Weak transcription	Fetal Heart	heart

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