Variant report

Variant	rs10165238
Chromosome Location	chr2:134286435-134286436
allele	G/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:25)

rs_ID	r²[population]
rs1016837	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1017366	0.82[CEU][hapmap]
rs10206425	0.82[CEU][hapmap]
rs11891880	0.82[CEU][hapmap];0.88[AMR][1000 genomes]
rs13399787	0.82[CEU][hapmap]
rs13408209	0.82[CEU][hapmap]
rs16825505	0.82[CEU][hapmap]
rs16826050	0.82[AMR][1000 genomes]
rs16826052	1.00[CEU][hapmap];0.82[AMR][1000 genomes]
rs17815418	0.82[CEU][hapmap]
rs61590587	0.95[ASN][1000 genomes]
rs6720995	0.82[CEU][hapmap]
rs6730679	0.82[CEU][hapmap]
rs6732077	0.82[AMR][1000 genomes]
rs72990470	0.82[AMR][1000 genomes]
rs72990471	0.82[AMR][1000 genomes]
rs73003138	0.85[AMR][1000 genomes]
rs73003141	0.85[AMR][1000 genomes]
rs73003144	0.82[AMR][1000 genomes]
rs73003146	0.85[AMR][1000 genomes]
rs73003147	0.82[AMR][1000 genomes]
rs7340446	1.00[CEU][hapmap]
rs7340510	0.82[CEU][hapmap];0.82[AMR][1000 genomes]
rs73960259	0.97[ASN][1000 genomes]
rs9917399	0.82[CEU][hapmap];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2830192	chr2:134259612-134311713	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134268200-134290000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:134282600-134299200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:134284200-134286600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:134285000-134290800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:134285800-134286600	Enhancers	Fetal Heart	heart
6	chr2:134286200-134286600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:134286200-134311600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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