Variant report

Variant	rs458581
Chromosome Location	chr5:75949635-75949636
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1423605	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2252231	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2431361	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2431362	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2431363	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2431364	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2431366	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432186	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432187	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2432188	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432189	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2455213	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2455215	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2455234	0.92[ASN][1000 genomes]
rs399058	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs429703	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs430389	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs456572	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs456708	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs457054	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs457182	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs457205	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs458573	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs458661	0.97[ASN][1000 genomes]
rs460374	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460431	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460482	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460562	0.94[ASN][1000 genomes]
rs461187	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs461273	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs461475	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs462587	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs463147	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs463973	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465988	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs466393	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs615951	0.99[ASN][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	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1035135	chr5:75927027-76092058	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75882600-75969400	Weak transcription	Stomach Mucosa	stomach
2	chr5:75914200-75953800	Weak transcription	Colonic Mucosa	Colon
3	chr5:75919200-75955400	Weak transcription	Fetal Kidney	kidney
4	chr5:75943800-75986600	Weak transcription	Gastric	stomach
5	chr5:75944400-75949800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:75945000-75950600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr5:75945200-75951000	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr5:75945200-75976200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr5:75945200-75976400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:75945200-76001000	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr5:75945600-75976600	Strong transcription	Liver	Liver
12	chr5:75945800-75970400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:75946000-75951000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:75946000-75953000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:75946000-75953000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:75946000-75953000	Weak transcription	Duodenum Mucosa	Duodenum
17	chr5:75946000-75953000	Weak transcription	Spleen	Spleen
18	chr5:75946000-75953800	Weak transcription	Pancreas	Pancrea
19	chr5:75946000-75953800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:75946000-75955200	Weak transcription	Aorta	Aorta
21	chr5:75946000-75958600	Weak transcription	Fetal Stomach	stomach
22	chr5:75946000-75959000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:75946000-75967000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:75946200-75950400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:75946200-75953600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr5:75946200-75953800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr5:75946200-75954000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:75946200-75954200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr5:75946200-75954200	Weak transcription	Fetal Thymus	thymus
30	chr5:75946200-75954400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:75946200-75954400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:75946200-75954400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr5:75946200-75976000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:75946400-76001000	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr5:75946600-75975000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:75946800-75953000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:75947000-75950400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr5:75947000-75970600	Weak transcription	Small Intestine	intestine
39	chr5:75947800-75981800	Strong transcription	Primary T cells from cord blood	blood
40	chr5:75947800-75992000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:75948000-75952200	Strong transcription	Primary hematopoietic stem cells	blood
42	chr5:75948000-75976200	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr5:75948000-75976200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr5:75948000-75976400	Strong transcription	Placenta	Placenta
45	chr5:75948000-76004600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr5:75948400-75950800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr5:75948400-75967000	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr5:75948600-75952400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr5:75948600-75958400	Strong transcription	Primary B cells from cord blood	blood
50	chr5:75948600-75958600	Weak transcription	Fetal Intestine Small	intestine

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