Variant report

Variant	rs10881072
Chromosome Location	chr12:47585115-47585116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:47579082..47584431-chr12:47584905..47587812,5	K562	blood:
2	chr12:47498470..47501746-chr12:47583705..47586367,3	MCF-7	breast:
3	chr12:47583159..47586380-chr12:47586604..47590176,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263838	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10748464	0.92[CEU][hapmap];0.92[MEX][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10785664	0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10785665	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10785666	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10785667	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10785668	0.91[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.85[TSI][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10881064	0.81[JPT][hapmap]
rs10881066	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10881067	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10881069	0.87[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10881070	0.91[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10881074	0.96[CEU][hapmap]
rs1404817	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1404818	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4768143	0.91[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4768778	0.87[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4768779	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4768780	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4768781	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs832733	0.84[CEU][hapmap]

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	nsv469368	chr12:47374908-47675680	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv558784	chr12:47374908-47675680	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv832399	chr12:47502910-47689601	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2751100	chr12:47541390-47746157	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47578200-47587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:47580800-47585600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr12:47581000-47585800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:47581800-47594000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr12:47582000-47585400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr12:47582200-47585400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:47582200-47585600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr12:47582400-47585200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:47582400-47585400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:47582400-47585400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr12:47582400-47585400	Enhancers	NHEK	skin
12	chr12:47582600-47585400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr12:47582800-47585400	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr12:47582800-47585800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:47583000-47585800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr12:47583200-47587200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:47583200-47587600	Weak transcription	Pancreas	Pancrea
18	chr12:47583200-47588400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:47583200-47589200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:47583200-47628600	Weak transcription	Aorta	Aorta
21	chr12:47583400-47585200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr12:47583400-47588000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:47583400-47588400	Weak transcription	Rectal Smooth Muscle	rectum
24	chr12:47583600-47585400	Enhancers	HMEC	breast
25	chr12:47583600-47585600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr12:47583800-47585200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr12:47583800-47585200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:47583800-47585200	Weak transcription	Colonic Mucosa	Colon
29	chr12:47583800-47585200	Weak transcription	Small Intestine	intestine
30	chr12:47583800-47587600	Weak transcription	Lung	lung
31	chr12:47584000-47600600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr12:47584200-47587000	Weak transcription	Psoas Muscle	Psoas
33	chr12:47584200-47587600	Weak transcription	Right Atrium	heart
34	chr12:47584200-47589600	Enhancers	Primary B cells from peripheral blood	blood
35	chr12:47584400-47586000	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr12:47584600-47585200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr12:47584600-47585400	Enhancers	Primary T cells from cord blood	blood
38	chr12:47584600-47585600	Enhancers	Primary T cells fromperipheralblood	blood
39	chr12:47584600-47585600	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr12:47584600-47585600	Weak transcription	Liver	Liver
41	chr12:47584600-47586600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr12:47584600-47587000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr12:47584600-47587000	Weak transcription	Spleen	Spleen
44	chr12:47584600-47587200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr12:47584600-47587400	Weak transcription	Primary hematopoietic stem cells	blood
46	chr12:47584600-47587600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:47584600-47588400	Weak transcription	Adipose Nuclei	Adipose
48	chr12:47584800-47585200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:47584800-47585200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:47584800-47585200	Enhancers	Primary T helper cells PMA-I stimulated	--

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