Variant report

Variant	rs17569923
Chromosome Location	chr1:92089160-92089161
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10518499	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11165059	0.80[EUR][1000 genomes]
rs11165064	0.84[EUR][1000 genomes]
rs12132074	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12135487	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17504418	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17569909	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17569956	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2478177	0.95[EUR][1000 genomes]
rs55996639	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59072552	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59178722	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72712451	0.84[EUR][1000 genomes]
rs72712461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949516	chr1:91644418-92109261	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	esv2763581	chr1:92068967-92203803	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1014990	chr1:92084142-92206674	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92084000-92103200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr1:92086600-92089200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:92087000-92089400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:92087400-92089200	Enhancers	Brain Angular Gyrus	brain
5	chr1:92088000-92089200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:92088000-92089400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:92088000-92089800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:92088800-92091600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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