Variant report

Variant	rs1927112
Chromosome Location	chr9:72740974-72740975
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	chr9:72733654..72736603-chr9:72737665..72741649,3	MCF-7	breast:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10114223	0.93[AMR][1000 genomes]
rs10511981	1.00[EUR][1000 genomes]
rs10735584	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10868800	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.87[TSI][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes]
rs11142364	0.94[YRI][hapmap];0.87[AMR][1000 genomes]
rs11142372	0.87[AMR][1000 genomes]
rs11521805	0.87[AMR][1000 genomes]
rs1180080	0.87[AMR][1000 genomes]
rs1180084	0.81[YRI][hapmap];0.87[AMR][1000 genomes]
rs1180089	0.86[ASW][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.81[YRI][hapmap];0.87[AMR][1000 genomes]
rs1180097	0.87[AMR][1000 genomes]
rs1180100	0.86[ASW][hapmap];0.92[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap];0.87[AMR][1000 genomes]
rs1180110	0.90[YRI][hapmap]
rs1180113	0.95[YRI][hapmap];0.87[AMR][1000 genomes]
rs1180119	0.94[YRI][hapmap];0.87[AMR][1000 genomes]
rs1183311	0.87[AMR][1000 genomes]
rs17052678	0.90[YRI][hapmap];0.87[AMR][1000 genomes]
rs1888155	0.87[AMR][1000 genomes]
rs1927094	0.81[YRI][hapmap];0.87[AMR][1000 genomes]
rs1927108	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1927109	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1927114	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1927123	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1927138	1.00[AMR][1000 genomes]
rs1927140	0.93[AMR][1000 genomes]
rs1927141	0.93[AMR][1000 genomes]
rs1927145	1.00[AMR][1000 genomes]
rs1927146	0.93[AMR][1000 genomes]
rs1927148	0.81[YRI][hapmap]
rs1998972	1.00[EUR][1000 genomes]
rs2148854	0.93[AMR][1000 genomes]
rs2148855	0.93[AMR][1000 genomes]
rs2148860	0.98[EUR][1000 genomes]
rs2182733	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2209781	0.93[AMR][1000 genomes]
rs2225128	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2309601	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2309637	0.93[AMR][1000 genomes]
rs2309641	1.00[AMR][1000 genomes]
rs2309645	0.86[ASW][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes]
rs2309646	0.87[AMR][1000 genomes]
rs2871297	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2997683	0.84[GIH][hapmap]
rs3015215	0.84[GIH][hapmap]
rs4744587	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4744980	1.00[EUR][1000 genomes]
rs4744985	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7020575	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7042675	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs72712293	0.87[AMR][1000 genomes]
rs72712300	0.87[AMR][1000 genomes]
rs7341691	0.87[AMR][1000 genomes]
rs7848955	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7857325	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7865289	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9410662	0.87[AMR][1000 genomes]
rs943535	0.86[ASW][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes]
rs943538	1.00[EUR][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	nsv1049457	chr9:72539144-72765913	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv949052	chr9:72698039-72741247	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72714800-72742400	Weak transcription	Aorta	Aorta
2	chr9:72722000-72758400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:72724400-72742600	Weak transcription	Right Ventricle	heart
4	chr9:72725600-72745200	Weak transcription	Lung	lung
5	chr9:72725800-72742600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr9:72725800-72764200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:72726200-72741000	Weak transcription	Fetal Stomach	stomach
8	chr9:72726200-72749200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr9:72726800-72785200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:72727000-72776200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr9:72727200-72746600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:72728200-72752800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr9:72728200-72758400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr9:72728600-72746800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr9:72729200-72744800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr9:72731200-72768400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:72733200-72741000	Weak transcription	Left Ventricle	heart
18	chr9:72733200-72745000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:72733800-72748400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:72736200-72741000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:72736200-72741000	Weak transcription	Right Atrium	heart
22	chr9:72736200-72745000	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr9:72736200-72746000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr9:72736200-72747400	Weak transcription	Fetal Muscle Leg	muscle
25	chr9:72736200-72748800	Weak transcription	Fetal Brain Female	brain
26	chr9:72736200-72761200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr9:72736400-72741200	Weak transcription	Psoas Muscle	Psoas
28	chr9:72736600-72744600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr9:72737000-72744200	Strong transcription	Colon Smooth Muscle	Colon
30	chr9:72737000-72748000	Strong transcription	Stomach Smooth Muscle	stomach
31	chr9:72737200-72745200	Strong transcription	HSMMtube	muscle
32	chr9:72737400-72741000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:72737400-72741200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:72737400-72741200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr9:72737600-72741000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:72737600-72741200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:72737600-72741200	Weak transcription	NHDF-Ad	bronchial
38	chr9:72737600-72741200	Weak transcription	Osteobl	bone
39	chr9:72737600-72741400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr9:72737600-72741400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:72737800-72742000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr9:72738000-72742600	Enhancers	HepG2	liver
43	chr9:72738200-72750400	Weak transcription	Fetal Intestine Small	intestine
44	chr9:72738400-72741800	Enhancers	Pancreas	Pancrea
45	chr9:72739000-72749000	Weak transcription	Gastric	stomach
46	chr9:72739600-72741600	Strong transcription	Adipose Nuclei	Adipose
47	chr9:72739800-72741600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr9:72739800-72741600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:72739800-72741800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:72740000-72741000	Weak transcription	Spleen	Spleen

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