Variant report

Variant	rs11169643
Chromosome Location	chr12:51363683-51363684
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:51358502..51360086-chr12:51361508..51364420,2	K562	blood:
2	chr12:51363073..51365710-chr12:51419692..51421851,2	MCF-7	breast:
3	chr12:51358068..51360086-chr12:51362108..51364420,3	K562	blood:

Variant related genes	Relation type
ENSG00000110911	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10876122	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11169625	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11169629	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]
rs11169634	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11169640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169651	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11169653	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11169658	1.00[CHB][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11169662	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11169674	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11169675	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11169708	1.00[GIH][hapmap];0.91[LWK][hapmap];0.86[MKK][hapmap];0.81[TSI][hapmap]
rs12227734	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1982777	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2016533	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2239860	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2269682	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2269683	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2452795	1.00[GIH][hapmap];0.81[TSI][hapmap]
rs2640525	1.00[GIH][hapmap];0.81[TSI][hapmap]
rs2640526	0.81[TSI][hapmap]
rs3809320	0.95[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4768871	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4768957	1.00[GIH][hapmap];1.00[LWK][hapmap];0.82[MKK][hapmap];0.81[TSI][hapmap]
rs7295893	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7399214	1.00[GIH][hapmap];0.81[TSI][hapmap]
rs8490	1.00[GIH][hapmap];0.92[LWK][hapmap];0.89[MKK][hapmap];0.90[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	nsv1053466	chr12:51350285-51375969	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

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	chr12:51331800-51382000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:51331800-51382000	Weak transcription	Ovary	ovary
8	chr12:51332600-51365000	Weak transcription	Fetal Brain Female	brain
9	chr12:51341600-51378200	Weak transcription	Right Ventricle	heart
10	chr12:51341800-51372600	Weak transcription	Osteobl	bone
11	chr12:51341800-51383200	Weak transcription	Fetal Brain Male	brain
12	chr12:51342400-51373200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:51342800-51378400	Weak transcription	NHLF	lung
14	chr12:51343000-51366200	Weak transcription	Brain Germinal Matrix	brain
15	chr12:51343600-51366200	Weak transcription	Gastric	stomach
16	chr12:51344000-51382000	Weak transcription	Esophagus	oesophagus
17	chr12:51344600-51381600	Weak transcription	Spleen	Spleen
18	chr12:51347200-51378000	Weak transcription	Brain Angular Gyrus	brain
19	chr12:51347400-51378000	Weak transcription	Brain Anterior Caudate	brain
20	chr12:51350800-51380600	Weak transcription	Fetal Lung	lung
21	chr12:51351200-51365200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:51354200-51365200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:51354400-51365200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:51354400-51365200	Weak transcription	Dnd41	blood
25	chr12:51354400-51383800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr12:51354600-51364200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:51355200-51365200	Weak transcription	HSMM	muscle
28	chr12:51355600-51378000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr12:51355800-51366200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr12:51355800-51378000	Weak transcription	A549	lung
31	chr12:51356000-51365200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:51356000-51372600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr12:51357600-51378000	Weak transcription	Psoas Muscle	Psoas
34	chr12:51358200-51366200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr12:51358400-51365200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr12:51358800-51364400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:51358800-51377800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:51359600-51365200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:51359800-51380400	Weak transcription	Fetal Kidney	kidney
40	chr12:51360000-51364200	Strong transcription	Primary T cells from cord blood	blood
41	chr12:51360000-51366400	Strong transcription	Fetal Thymus	thymus
42	chr12:51360200-51363800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:51360200-51365600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:51360200-51374400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr12:51360200-51381800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:51360400-51365200	Weak transcription	Liver	Liver
47	chr12:51360400-51365800	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr12:51360400-51372600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:51360400-51374400	Weak transcription	HUVEC	blood vessel
50	chr12:51360600-51365200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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