Variant report

Variant	rs62038316
Chromosome Location	chr16:82362872-82362873
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:82342573..82345161-chr16:82362361..82364384,2	MCF-7	breast:
2	chr16:82297332..82297930-chr16:82362205..82363171,2	MCF-7	breast:
3	chr16:82358580..82360925-chr16:82361830..82364617,5	MCF-7	breast:
4	chr16:82297678..82300099-chr16:82362624..82364703,2	MCF-7	breast:
5	chr16:82361874..82363383-chr16:82377438..82379886,2	MCF-7	breast:
6	chr16:82362203..82364842-chr16:82370219..82372533,4	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs13331162	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13331990	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13336423	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13336467	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13337515	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13337698	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2906801	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2906804	0.80[ASN][1000 genomes]
rs2906805	0.83[ASN][1000 genomes]
rs2906806	0.80[ASN][1000 genomes]
rs2906808	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2932831	0.82[ASN][1000 genomes]
rs2967411	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2967417	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2967418	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2967421	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3887923	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55807838	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56174352	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58226947	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59325078	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61687651	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62038310	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62038311	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62038313	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62038317	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62038318	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62038319	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62038320	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62038321	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62038322	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62038324	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66726226	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7190770	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7197429	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs732757	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs745256	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs977768	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs977769	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9926445	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9932426	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9935462	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9937707	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv833302	chr16:82188351-82363863	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	esv1844598	chr16:82195234-82429790	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
6	esv1847414	chr16:82195234-82429790	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1065896	chr16:82213517-82731994	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv833304	chr16:82306875-82429021	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv525789	chr16:82349244-82402803	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82361800-82364000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr16:82362400-82363800	Enhancers	Pancreas	Pancrea
3	chr16:82362600-82363200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr16:82362600-82364200	Enhancers	Liver	Liver
5	chr16:82362600-82365000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr16:82362600-82365000	Enhancers	HepG2	liver
7	chr16:82362600-82366200	Enhancers	Stomach Mucosa	stomach
8	chr16:82362800-82363000	Enhancers	Brain Anterior Caudate	brain
9	chr16:82362800-82363000	Enhancers	Brain Cingulate Gyrus	brain
10	chr16:82362800-82363400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr16:82362800-82363600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:82362800-82363600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr16:82362800-82363600	Enhancers	Gastric	stomach
14	chr16:82362800-82363800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr16:82362800-82363800	Enhancers	Psoas Muscle	Psoas
16	chr16:82362800-82364200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr16:82362800-82364400	Enhancers	Brain Hippocampus Middle	brain
18	chr16:82362800-82364400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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