Variant report

Variant	rs7824892
Chromosome Location	chr8:104626979-104626980
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10086733	0.81[YRI][hapmap]
rs10096428	0.83[AFR][1000 genomes]
rs10102523	0.81[YRI][hapmap]
rs10505043	0.81[YRI][hapmap]
rs12114100	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12115119	1.00[AMR][1000 genomes]
rs13249634	0.85[YRI][hapmap]
rs13257474	0.81[YRI][hapmap]
rs13263630	0.87[AFR][1000 genomes]
rs13439770	0.83[YRI][hapmap]
rs16870614	0.85[YRI][hapmap]
rs16870616	0.85[YRI][hapmap]
rs17234389	0.85[YRI][hapmap]
rs28799635	0.83[AFR][1000 genomes]
rs35400024	0.82[AFR][1000 genomes]
rs55967316	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56773931	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57067672	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57888580	1.00[AMR][1000 genomes]
rs58003496	1.00[AMR][1000 genomes]
rs58032159	1.00[AMR][1000 genomes]
rs58222629	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58774639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60299412	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60412815	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60552383	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61042766	1.00[AMR][1000 genomes]
rs61589769	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6468877	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6985351	0.85[YRI][hapmap]
rs6986085	0.81[YRI][hapmap]
rs6986283	0.83[YRI][hapmap]
rs6993163	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6997310	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7003753	0.84[AFR][1000 genomes]
rs7006816	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7015973	0.81[AFR][1000 genomes]
rs73696666	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73696667	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697653	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697657	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697662	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697668	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697673	1.00[AMR][1000 genomes]
rs73697683	1.00[AMR][1000 genomes]
rs73697684	1.00[AMR][1000 genomes]
rs73700411	1.00[AMR][1000 genomes]
rs73700412	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73700420	0.89[AFR][1000 genomes]
rs73701882	1.00[AMR][1000 genomes]
rs73701884	0.81[AFR][1000 genomes]
rs73702146	1.00[AMR][1000 genomes]
rs73702149	1.00[AMR][1000 genomes]
rs7825848	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7826206	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7830015	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7833129	0.81[YRI][hapmap]
rs7841801	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7843933	1.00[AMR][1000 genomes]
rs7845290	0.80[YRI][hapmap]
rs9297332	0.81[YRI][hapmap]
rs9297333	0.80[YRI][hapmap]
rs9297334	0.81[YRI][hapmap]
rs9297335	0.81[YRI][hapmap]
rs9918740	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv1032085	chr8:104362187-104878345	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1034183	chr8:104369940-104814008	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv539707	chr8:104369940-104814008	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv1016387	chr8:104578389-104931853	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 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	chr8:104619600-104634800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:104623000-104632600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:104625200-104627800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr8:104625200-104629000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr8:104626000-104627200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr8:104626200-104628200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:104626800-104627000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:104626800-104628800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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