Variant report

Variant	rs58591737
Chromosome Location	chr5:177645574-177645575
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1134369	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11743721	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11750481	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17080447	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17639362	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17759	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55653122	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72817294	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72819004	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7705559	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7705704	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	126 gene(s)	inside rSNPs	diseases
4	nsv482872	chr5:177580298-177744381	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	106 gene(s)	inside rSNPs	diseases
5	nsv1021981	chr5:177620372-177825272	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
6	nsv537967	chr5:177620372-177825272	Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
7	nsv1024689	chr5:177638936-177926244	Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv537968	chr5:177638936-177926244	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	esv3425423	chr5:177643496-177648394	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177634000-177650800	Strong transcription	Placenta	Placenta
2	chr5:177634400-177654200	Strong transcription	Fetal Stomach	stomach
3	chr5:177634600-177646000	Strong transcription	Thymus	Thymus
4	chr5:177634800-177645800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:177635000-177647000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:177635000-177650200	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:177635000-177650400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:177635000-177650400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:177635000-177650400	Strong transcription	Adipose Nuclei	Adipose
10	chr5:177635200-177646000	Strong transcription	NH-A	brain
11	chr5:177635400-177646200	Strong transcription	Osteobl	bone
12	chr5:177635400-177646400	Strong transcription	Muscle Satellite Cultured Cells	--
13	chr5:177635400-177649200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:177635400-177651000	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr5:177635800-177657000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr5:177636000-177648000	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:177636000-177654000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:177639400-177657600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr5:177640000-177648400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:177640000-177650400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:177640400-177655600	Weak transcription	Right Atrium	heart
22	chr5:177641000-177650800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr5:177641600-177648400	Weak transcription	Small Intestine	intestine
24	chr5:177642000-177645800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr5:177642600-177646200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr5:177642600-177654200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:177642800-177647600	Weak transcription	K562	blood
28	chr5:177642800-177648200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr5:177643000-177646600	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr5:177643000-177647800	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr5:177643000-177648200	Weak transcription	Colonic Mucosa	Colon
32	chr5:177643200-177648000	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr5:177643200-177648200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr5:177643200-177651000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr5:177643400-177645800	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr5:177643400-177647600	Strong transcription	Primary T cells from cord blood	blood
37	chr5:177643400-177647600	Strong transcription	Fetal Intestine Small	intestine
38	chr5:177643400-177648400	Weak transcription	Gastric	stomach
39	chr5:177643400-177649400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:177643400-177650200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:177643400-177650600	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:177643400-177651600	Weak transcription	HSMMtube	muscle
43	chr5:177643400-177656400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:177643600-177647400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:177643600-177648200	Weak transcription	Brain Angular Gyrus	brain
46	chr5:177643600-177649600	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:177643600-177650400	Weak transcription	Fetal Heart	heart
48	chr5:177643600-177654400	Weak transcription	Aorta	Aorta
49	chr5:177643600-177655200	Weak transcription	Stomach Mucosa	stomach
50	chr5:177643800-177647600	Weak transcription	Fetal Kidney	kidney

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