Variant report

Variant	rs11176672
Chromosome Location	chr12:67685872-67685873
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:67678774..67680822-chr12:67683989..67686617,2	MCF-7	breast:
2	chr12:67685431..67687281-chr12:67692983..67694546,2	MCF-7	breast:
3	chr12:67662577..67664634-chr12:67685123..67686741,3	MCF-7	breast:
4	chr12:67680186..67682329-chr12:67685007..67687725,2	MCF-7	breast:
5	chr12:67673864..67678122-chr12:67685372..67688266,4	K562	blood:
6	chr12:67674261..67676215-chr12:67685675..67687691,2	MCF-7	breast:
7	chr12:67672008..67673697-chr12:67685020..67687108,2	K562	blood:

Variant related genes	Relation type
ENSG00000111530	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10128823	1.00[EUR][1000 genomes]
rs10129028	1.00[EUR][1000 genomes]
rs11176669	0.88[AFR][1000 genomes]
rs11176670	0.94[AFR][1000 genomes]
rs11176676	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11176679	1.00[EUR][1000 genomes]
rs11176684	1.00[EUR][1000 genomes]
rs11176691	1.00[EUR][1000 genomes]
rs11176692	1.00[EUR][1000 genomes]
rs11176693	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11176694	1.00[EUR][1000 genomes]
rs11176715	1.00[EUR][1000 genomes]
rs11176740	1.00[EUR][1000 genomes]
rs11503726	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12297966	1.00[EUR][1000 genomes]
rs12299042	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12299097	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12300582	1.00[EUR][1000 genomes]
rs12303089	1.00[EUR][1000 genomes]
rs12305377	0.95[AFR][1000 genomes]
rs12306375	1.00[EUR][1000 genomes]
rs12306657	0.94[AFR][1000 genomes]
rs12307363	1.00[EUR][1000 genomes]
rs12307464	1.00[EUR][1000 genomes]
rs12311491	1.00[EUR][1000 genomes]
rs12311797	1.00[EUR][1000 genomes]
rs12311840	1.00[EUR][1000 genomes]
rs12311845	1.00[EUR][1000 genomes]
rs12312040	1.00[EUR][1000 genomes]
rs12313282	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12314503	1.00[EUR][1000 genomes]
rs12315624	1.00[EUR][1000 genomes]
rs12318518	1.00[EUR][1000 genomes]
rs12318591	1.00[EUR][1000 genomes]
rs12318995	1.00[EUR][1000 genomes]
rs12320566	1.00[EUR][1000 genomes]
rs12321396	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12322901	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17103392	1.00[EUR][1000 genomes]
rs17103652	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17103772	1.00[EUR][1000 genomes]
rs17120707	1.00[EUR][1000 genomes]
rs17120710	1.00[EUR][1000 genomes]
rs3087577	0.87[AFR][1000 genomes]
rs4083304	1.00[EUR][1000 genomes]
rs57886620	1.00[EUR][1000 genomes]
rs61281993	0.87[AFR][1000 genomes]
rs61504642	1.00[EUR][1000 genomes]
rs6581751	1.00[EUR][1000 genomes]
rs7135195	1.00[EUR][1000 genomes]
rs7294827	1.00[EUR][1000 genomes]
rs7306853	1.00[EUR][1000 genomes]
rs7307643	1.00[EUR][1000 genomes]
rs7312079	1.00[EUR][1000 genomes]
rs73320752	1.00[EUR][1000 genomes]
rs73322616	1.00[EUR][1000 genomes]
rs73326445	1.00[EUR][1000 genomes]
rs73326448	1.00[EUR][1000 genomes]
rs73326466	1.00[EUR][1000 genomes]
rs7954050	0.89[AFR][1000 genomes]
rs7954999	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7962872	1.00[EUR][1000 genomes]
rs7964763	1.00[EUR][1000 genomes]
rs7966031	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7977574	1.00[EUR][1000 genomes]
rs9989007	1.00[EUR][1000 genomes]
rs9989023	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv541524	chr12:67311057-67700349	Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv559212	chr12:67373549-67850925	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1054111	chr12:67556780-67865542	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv525023	chr12:67672870-67708669	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67664800-67694400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:67664800-67699600	Weak transcription	Aorta	Aorta
3	chr12:67665200-67690200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:67665200-67699000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:67665400-67687600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:67666000-67688400	Weak transcription	Fetal Kidney	kidney
7	chr12:67666000-67701000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr12:67668400-67688200	Weak transcription	HUVEC	blood vessel
9	chr12:67670000-67688800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr12:67670000-67699200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr12:67670200-67698200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:67670400-67689600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:67670800-67688400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr12:67671000-67688800	Weak transcription	NHEK	skin
15	chr12:67671000-67689400	Weak transcription	NHLF	lung
16	chr12:67671200-67688200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr12:67671400-67698400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:67671600-67691800	Weak transcription	Fetal Brain Male	brain
19	chr12:67672200-67699000	Weak transcription	Esophagus	oesophagus
20	chr12:67672400-67693800	Weak transcription	Psoas Muscle	Psoas
21	chr12:67673200-67699400	Weak transcription	Small Intestine	intestine
22	chr12:67674200-67688800	Weak transcription	Brain Angular Gyrus	brain
23	chr12:67674200-67694000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr12:67674400-67696000	Weak transcription	Brain Hippocampus Middle	brain
25	chr12:67674600-67689800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:67674600-67708000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:67674800-67697800	Strong transcription	Fetal Thymus	thymus
28	chr12:67674800-67706400	Weak transcription	Stomach Mucosa	stomach
29	chr12:67675600-67694600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:67676200-67691000	Weak transcription	HMEC	breast
31	chr12:67676800-67691800	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr12:67678600-67699000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:67678800-67688400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr12:67679000-67686400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr12:67679000-67686600	Weak transcription	Osteobl	bone
36	chr12:67679000-67687600	Weak transcription	Adipose Nuclei	Adipose
37	chr12:67679000-67688000	Weak transcription	NHDF-Ad	bronchial
38	chr12:67679000-67692200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr12:67679600-67688200	Weak transcription	Placenta	Placenta
40	chr12:67679600-67692200	Weak transcription	Fetal Brain Female	brain
41	chr12:67679800-67687600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:67680000-67687200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr12:67680000-67696000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:67680600-67689800	Strong transcription	Fetal Intestine Large	intestine
45	chr12:67680800-67686400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:67680800-67686600	Strong transcription	Primary B cells from cord blood	blood
47	chr12:67680800-67687600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:67680800-67688200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:67681000-67686400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr12:67681000-67687600	Weak transcription	Rectal Mucosa Donor 29	rectum

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