Variant report

Variant	rs13133396
Chromosome Location	chr4:143673426-143673427
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10023146	1.00[ASN][1000 genomes]
rs10034956	1.00[ASN][1000 genomes]
rs10049507	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11100756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11725795	1.00[ASN][1000 genomes]
rs13103261	0.93[ASN][1000 genomes]
rs13105531	0.93[ASN][1000 genomes]
rs13106530	0.84[EUR][1000 genomes]
rs13108947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13112871	1.00[ASN][1000 genomes]
rs13115869	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13116732	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13132001	0.87[ASN][1000 genomes]
rs13135210	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13140998	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1373033	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1373664	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1441412	0.93[ASN][1000 genomes]
rs1441416	1.00[ASN][1000 genomes]
rs1899564	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2322814	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28367408	0.93[ASN][1000 genomes]
rs28410519	0.93[ASN][1000 genomes]
rs28421948	0.93[ASN][1000 genomes]
rs28453834	0.93[ASN][1000 genomes]
rs28462985	0.93[ASN][1000 genomes]
rs28508323	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28533753	0.93[ASN][1000 genomes]
rs28608029	1.00[ASN][1000 genomes]
rs28665985	0.93[ASN][1000 genomes]
rs28667040	0.93[ASN][1000 genomes]
rs28685292	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34032529	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34241470	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34412123	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34611963	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34804364	0.93[ASN][1000 genomes]
rs35053070	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35416729	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35838997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35918867	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36042265	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62331921	0.93[ASN][1000 genomes]
rs62331922	0.93[ASN][1000 genomes]
rs62331933	0.93[ASN][1000 genomes]
rs62331934	0.93[ASN][1000 genomes]
rs7662067	0.93[ASN][1000 genomes]
rs986081	1.00[ASN][1000 genomes]
rs9994239	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9994268	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830101	chr4:143518810-143684392	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv595606	chr4:143631691-143729595	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv880174	chr4:143639498-143848024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143671600-143674200	Enhancers	Fetal Heart	heart
2	chr4:143672200-143674400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:143672600-143674000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:143672600-143698400	Weak transcription	Aorta	Aorta
5	chr4:143672800-143674200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:143673000-143674200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:143673200-143673600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:143673200-143674000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:143673400-143673800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr4:143673400-143673800	Enhancers	Fetal Muscle Leg	muscle
11	chr4:143673400-143673800	Enhancers	HSMMtube	muscle
12	chr4:143673400-143674000	Enhancers	Ovary	ovary
13	chr4:143673400-143674200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:143673400-143674200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:143673400-143674200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:143673400-143674200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links