Variant report

Variant	rs11169629
Chromosome Location	chr12:51349444-51349445
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:51345899..51348517-chr12:51349158..51350888,2	MCF-7	breast:
2	chr12:51349059..51351972-chr12:51418064..51419809,2	K562	blood:

Variant related genes	Relation type
ENSG00000214511	Chromatin interaction
ENSG00000110911	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10876122	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11169625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11169634	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169640	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11169643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11169651	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11169653	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11169658	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11169662	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11169674	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11169675	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12227734	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1982777	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2016533	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2239860	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2269682	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2269683	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3809320	0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4768871	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7295893	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][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	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	esv34039	chr12:51326702-51671911	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51323000-51377200	Weak transcription	Aorta	Aorta
2	chr12:51328800-51378000	Weak transcription	Brain Substantia Nigra	brain
3	chr12:51329600-51373600	Weak transcription	Left Ventricle	heart
4	chr12:51331400-51378400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr12:51331600-51373800	Weak transcription	Pancreas	Pancrea
6	chr12:51331800-51353800	Weak transcription	Primary T cells from cord blood	blood
7	chr12:51331800-51382000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr12:51331800-51382000	Weak transcription	Ovary	ovary
9	chr12:51332600-51354400	Weak transcription	Thymus	Thymus
10	chr12:51332600-51365000	Weak transcription	Fetal Brain Female	brain
11	chr12:51340000-51361800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:51341600-51378200	Weak transcription	Right Ventricle	heart
13	chr12:51341800-51372600	Weak transcription	Osteobl	bone
14	chr12:51341800-51383200	Weak transcription	Fetal Brain Male	brain
15	chr12:51342200-51361200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr12:51342400-51360000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:51342400-51373200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:51342800-51378400	Weak transcription	NHLF	lung
19	chr12:51343000-51355400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr12:51343000-51366200	Weak transcription	Brain Germinal Matrix	brain
21	chr12:51343200-51361600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr12:51343400-51355200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:51343600-51366200	Weak transcription	Gastric	stomach
24	chr12:51344000-51361400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr12:51344000-51382000	Weak transcription	Esophagus	oesophagus
26	chr12:51344600-51381600	Weak transcription	Spleen	Spleen
27	chr12:51345000-51361200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:51345600-51354000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:51347000-51360600	Weak transcription	Fetal Stomach	stomach
30	chr12:51347000-51361200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:51347200-51360200	Weak transcription	Lung	lung
32	chr12:51347200-51361400	Weak transcription	Brain Hippocampus Middle	brain
33	chr12:51347200-51362000	Weak transcription	Fetal Muscle Leg	muscle
34	chr12:51347200-51378000	Weak transcription	Brain Angular Gyrus	brain
35	chr12:51347400-51360200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr12:51347400-51378000	Weak transcription	Brain Anterior Caudate	brain
37	chr12:51348000-51360400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:51349000-51360600	Weak transcription	Fetal Intestine Small	intestine
39	chr12:51349200-51363600	Weak transcription	Primary hematopoietic stem cells	blood

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