Variant report

Variant	rs73406245
Chromosome Location	chr15:53845646-53845647
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:53839734..53842688-chr15:53844777..53846540,2	K562	blood:
2	chr15:53839488..53841156-chr15:53845536..53848480,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs56021461	1.00[EUR][1000 genomes]
rs56087131	1.00[EUR][1000 genomes]
rs56270636	1.00[EUR][1000 genomes]
rs56318546	1.00[EUR][1000 genomes]
rs56375061	1.00[EUR][1000 genomes]
rs57715130	1.00[EUR][1000 genomes]
rs58089322	1.00[EUR][1000 genomes]
rs58528595	1.00[EUR][1000 genomes]
rs59180677	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60043908	1.00[EUR][1000 genomes]
rs60084149	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73406205	1.00[EUR][1000 genomes]
rs73406217	1.00[EUR][1000 genomes]
rs73406229	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73406234	1.00[EUR][1000 genomes]
rs73406236	1.00[EUR][1000 genomes]
rs73406271	1.00[EUR][1000 genomes]
rs73406272	1.00[EUR][1000 genomes]
rs73406274	1.00[EUR][1000 genomes]
rs74017404	1.00[EUR][1000 genomes]
rs74017409	1.00[EUR][1000 genomes]
rs74017411	1.00[EUR][1000 genomes]
rs74017421	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904223	chr15:53665247-54340070	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv904224	chr15:53668018-54210677	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1040216	chr15:53743780-53851679	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv833009	chr15:53752901-53935303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1038512	chr15:53803770-53851679	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv9267	chr15:53821005-54132612	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv569433	chr15:53828686-53860607	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv904225	chr15:53840665-53878948	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
11	esv275172	chr15:53841671-53849690	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
12	nsv569434	chr15:53845097-53860607	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
13	nsv569435	chr15:53845097-53966805	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53842400-53851000	Weak transcription	Liver	Liver
2	chr15:53842600-53847200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr15:53842600-53847400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr15:53842600-53851000	Weak transcription	Fetal Intestine Small	intestine
5	chr15:53843600-53852200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr15:53844200-53852200	Weak transcription	Small Intestine	intestine
7	chr15:53844600-53845800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:53845000-53845800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:53845600-53846600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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