Variant report

Variant	rs151944
Chromosome Location	chr5:36904399-36904400
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:36877627..36879271-chr5:36903588..36906365,2	MCF-7	breast:
2	chr5:36894674..36897624-chr5:36903658..36906079,2	K562	blood:
3	chr5:36903517..36905650-chr5:36910483..36913260,3	MCF-7	breast:
4	chr5:36899113..36901720-chr5:36902343..36906558,3	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs12657771	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13158310	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13170811	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13176880	0.84[EUR][1000 genomes]
rs13180309	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1466862	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs150380	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs158622	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs158623	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs158624	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs158791	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs158796	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs158803	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs159749	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159751	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs159753	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs159755	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs159913	0.88[EUR][1000 genomes]
rs168662	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs184182	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs186173	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs188541	0.86[EUR][1000 genomes]
rs292182	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs292183	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs292184	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs292194	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs292195	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs296962	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs300049	0.83[EUR][1000 genomes]
rs300051	0.83[EUR][1000 genomes]
rs300053	0.85[EUR][1000 genomes]
rs300055	0.87[EUR][1000 genomes]
rs300058	0.88[EUR][1000 genomes]
rs300060	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs300061	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs300063	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs300064	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs300065	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs301859	0.87[EUR][1000 genomes]
rs301901	0.87[EUR][1000 genomes]
rs301917	0.87[EUR][1000 genomes]
rs3104057	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs388098	0.87[EUR][1000 genomes]
rs6875748	0.88[EUR][1000 genomes]
rs6899155	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv532133	chr5:36834932-36906436	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
5	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv830264	chr5:36887002-36941494	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36886400-36904800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr5:36886600-36904800	Weak transcription	Right Ventricle	heart
3	chr5:36886600-36909200	Weak transcription	Left Ventricle	heart
4	chr5:36886600-36910400	Weak transcription	Ovary	ovary
5	chr5:36888200-36910400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:36888800-36911000	Weak transcription	Fetal Lung	lung
7	chr5:36895800-36918800	Weak transcription	Small Intestine	intestine
8	chr5:36895800-36928600	Weak transcription	HSMM	muscle
9	chr5:36896200-36908000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:36896400-36904600	Weak transcription	Primary T cells from cord blood	blood
11	chr5:36896600-36904400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr5:36898000-36907200	Weak transcription	Stomach Mucosa	stomach
13	chr5:36898400-36905600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr5:36899000-36926400	Weak transcription	Gastric	stomach
15	chr5:36900200-36908400	Weak transcription	Colon Smooth Muscle	Colon
16	chr5:36900600-36904600	Weak transcription	Psoas Muscle	Psoas
17	chr5:36900600-36904800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr5:36901000-36904600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:36901000-36908800	Weak transcription	Fetal Heart	heart
20	chr5:36901200-36904600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr5:36902000-36911400	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr5:36902600-36912800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:36902800-36904800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr5:36902800-36904800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr5:36902800-36908200	Weak transcription	Brain Hippocampus Middle	brain
26	chr5:36902800-36912600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr5:36903200-36905200	Enhancers	Primary B cells from peripheral blood	blood
28	chr5:36903200-36906200	Weak transcription	Thymus	Thymus
29	chr5:36903400-36904400	Weak transcription	Primary B cells from cord blood	blood
30	chr5:36903400-36904800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:36903600-36908400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:36903800-36919200	Weak transcription	K562	blood
33	chr5:36904000-36904400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr5:36904000-36905600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr5:36904200-36905000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:36904200-36905000	Enhancers	Primary T cells fromperipheralblood	blood
37	chr5:36904200-36905000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr5:36904200-36905200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:36904200-36905200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr5:36904200-36905600	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr5:36904200-36914600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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