Variant report

Variant	rs7712558
Chromosome Location	chr5:37107263-37107264
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10061157	0.91[YRI][hapmap]
rs10473039	1.00[CHD][hapmap]
rs12518867	1.00[CHB][hapmap]
rs301863	0.84[YRI][hapmap]
rs55780492	1.00[AMR][1000 genomes]
rs59075952	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59763526	1.00[AMR][1000 genomes]
rs61745362	1.00[AMR][1000 genomes]
rs6859950	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6864648	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6868809	0.84[YRI][hapmap]
rs6876937	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6886211	0.92[AFR][1000 genomes]
rs73750914	1.00[AMR][1000 genomes]
rs73750922	1.00[AMR][1000 genomes]
rs73750926	1.00[AMR][1000 genomes]
rs73750953	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	nsv917880	chr5:36948778-37115342	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
8	esv1802391	chr5:36958598-37242600	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv597822	chr5:36997953-37147152	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
11	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37065000-37107600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr5:37067000-37111400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr5:37080200-37112000	Weak transcription	Fetal Heart	heart
4	chr5:37082000-37109000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr5:37082800-37169200	Weak transcription	Spleen	Spleen
6	chr5:37087200-37113600	Weak transcription	NH-A	brain
7	chr5:37099400-37107600	Weak transcription	Gastric	stomach
8	chr5:37100800-37112000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr5:37101200-37107600	Weak transcription	Right Ventricle	heart
10	chr5:37101200-37115000	Weak transcription	A549	lung
11	chr5:37101400-37113400	Weak transcription	Brain Substantia Nigra	brain
12	chr5:37102200-37107600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr5:37102200-37108000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr5:37102200-37114400	Weak transcription	HMEC	breast
15	chr5:37102600-37107600	Weak transcription	Psoas Muscle	Psoas
16	chr5:37102600-37109400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:37102600-37115800	Strong transcription	HSMM	muscle
18	chr5:37102600-37121600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:37102800-37107600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr5:37102800-37110800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr5:37102800-37111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr5:37102800-37112200	Weak transcription	HUVEC	blood vessel
23	chr5:37102800-37114200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr5:37103000-37107400	Weak transcription	Brain Anterior Caudate	brain
25	chr5:37103000-37108600	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr5:37103000-37109200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:37103000-37109400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr5:37103000-37110000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:37103000-37110000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:37103000-37113200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:37103200-37110000	Strong transcription	Adipose Nuclei	Adipose
32	chr5:37103400-37108400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:37103400-37108800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr5:37103400-37109000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr5:37103600-37108400	Weak transcription	Colonic Mucosa	Colon
36	chr5:37103600-37115800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr5:37103600-37135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:37103800-37109000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr5:37103800-37109200	Weak transcription	Primary T cells from cord blood	blood
40	chr5:37103800-37113600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:37103800-37143200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr5:37104000-37107600	Weak transcription	NHDF-Ad	bronchial
43	chr5:37104000-37110800	Strong transcription	Fetal Brain Female	brain
44	chr5:37104200-37109400	Strong transcription	Fetal Lung	lung
45	chr5:37104200-37110600	Weak transcription	GM12878-XiMat	blood
46	chr5:37104400-37108800	Weak transcription	Thymus	Thymus
47	chr5:37104800-37110000	Strong transcription	Stomach Smooth Muscle	stomach
48	chr5:37104800-37113400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr5:37105200-37119000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:37105400-37107400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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