Variant report

Variant	rs7165145
Chromosome Location	chr15:31700452-31700453
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10047980	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10851546	0.97[EUR][1000 genomes]
rs11071016	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4261489	0.98[EUR][1000 genomes]
rs4328401	0.97[EUR][1000 genomes]
rs4354896	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4389106	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4586393	0.98[EUR][1000 genomes]
rs4779873	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4779874	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62037901	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6493635	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6493639	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6493659	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7171213	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7174005	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7175258	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7182014	0.86[EUR][1000 genomes]
rs7402619	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]

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	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv932896	chr15:31292475-31730445	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	esv34100	chr15:31496514-31792591	Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv903840	chr15:31589970-31800149	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv903843	chr15:31672947-31723279	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31696400-31700600	Enhancers	Primary B cells from cord blood	blood
2	chr15:31696400-31704200	Weak transcription	HMEC	breast
3	chr15:31696600-31704200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:31698200-31704200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:31698400-31700600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr15:31699200-31700800	Enhancers	Monocytes-CD14+_RO01746	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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