Variant report

Variant	rs501544
Chromosome Location	chr5:80301652-80301653
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs481785	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs483970	0.86[CEU][hapmap];0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs497522	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs499090	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs509741	0.87[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs516660	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs521812	0.83[ASN][1000 genomes]
rs527116	0.87[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs527506	0.86[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs533308	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs535083	0.83[ASN][1000 genomes]
rs538957	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs539809	0.86[CEU][hapmap];0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs546746	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs555979	0.83[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs564459	0.81[ASN][1000 genomes]
rs565476	0.86[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs565834	0.90[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs567367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs569262	0.81[CEU][hapmap];0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs570858	0.86[CEU][hapmap];0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs577470	0.81[ASN][1000 genomes]
rs6453538	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv598747	chr5:79996632-80322712	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1021784	chr5:80023679-80313586	ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv537787	chr5:80023679-80313586	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv830358	chr5:80197105-80358920	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv830360	chr5:80283278-80446040	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv4897	chr5:80284196-80330223	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80291400-80302400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr5:80294800-80302400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr5:80298400-80302200	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr5:80299400-80302200	Enhancers	Primary T cells fromperipheralblood	blood
5	chr5:80299400-80302400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:80299600-80302200	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr5:80299600-80302400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr5:80299600-80302400	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr5:80299600-80304400	Enhancers	Fetal Thymus	thymus
10	chr5:80300000-80313000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:80300200-80302000	Weak transcription	Dnd41	blood
12	chr5:80300200-80302200	Weak transcription	HepG2	liver
13	chr5:80300200-80302400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:80300400-80302200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr5:80300400-80302200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr5:80300400-80302400	Weak transcription	Right Atrium	heart
17	chr5:80300400-80302800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:80300400-80304800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:80300400-80312800	Weak transcription	Brain Hippocampus Middle	brain
20	chr5:80300400-80316600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:80300400-80318400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr5:80300600-80302000	Enhancers	Primary T cells from cord blood	blood
23	chr5:80300600-80302000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr5:80300600-80302000	Weak transcription	Thymus	Thymus
25	chr5:80300600-80302600	Weak transcription	Brain Angular Gyrus	brain
26	chr5:80300600-80303400	Weak transcription	Brain Substantia Nigra	brain
27	chr5:80300800-80306200	Weak transcription	Fetal Lung	lung
28	chr5:80301000-80302400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:80301000-80302600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr5:80301200-80302400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr5:80301200-80303000	Weak transcription	Adipose Nuclei	Adipose
32	chr5:80301400-80302400	Weak transcription	Left Ventricle	heart
33	chr5:80301600-80305000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links