Variant report

Variant	rs8048713
Chromosome Location	chr16:82047784-82047785
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs11865006	0.86[AMR][1000 genomes]
rs13333646	0.91[AMR][1000 genomes]
rs13333826	0.91[AMR][1000 genomes]
rs13334514	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16956130	1.00[ASN][1000 genomes]
rs16956155	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16956161	0.94[ASN][1000 genomes]
rs16956174	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16956191	1.00[ASN][1000 genomes]
rs16956202	0.94[ASN][1000 genomes]
rs16956236	0.82[AMR][1000 genomes]
rs16956242	0.86[AMR][1000 genomes]
rs28448747	0.95[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28558197	0.95[AMR][1000 genomes]
rs34132140	0.91[AMR][1000 genomes]
rs36043523	0.94[ASN][1000 genomes]
rs41530451	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4262939	0.91[AMR][1000 genomes]
rs4316745	0.94[ASN][1000 genomes]
rs4354930	0.94[ASN][1000 genomes]
rs4476172	0.94[ASN][1000 genomes]
rs4536470	0.94[ASN][1000 genomes]
rs4541072	0.83[ASN][1000 genomes]
rs4580158	0.94[ASN][1000 genomes]
rs4591137	0.94[ASN][1000 genomes]
rs4636900	0.94[ASN][1000 genomes]
rs57566286	0.86[AMR][1000 genomes]
rs58097356	0.83[ASN][1000 genomes]
rs59151852	0.86[AMR][1000 genomes]
rs59961458	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59976110	0.94[ASN][1000 genomes]
rs60200374	0.91[AMR][1000 genomes]
rs61644377	0.94[ASN][1000 genomes]
rs6564956	0.94[ASN][1000 genomes]
rs6564957	0.83[ASN][1000 genomes]
rs6564960	1.00[AMR][1000 genomes]
rs7187298	0.94[ASN][1000 genomes]
rs7188332	0.82[AMR][1000 genomes]
rs7193161	1.00[AMR][1000 genomes]
rs7193258	0.88[ASN][1000 genomes]
rs7194226	0.94[ASN][1000 genomes]
rs7195977	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7198264	0.86[AMR][1000 genomes]
rs7201738	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7202378	0.86[AMR][1000 genomes]
rs7202626	0.94[ASN][1000 genomes]
rs7205983	0.94[ASN][1000 genomes]
rs7206672	0.94[ASN][1000 genomes]
rs73598796	0.94[ASN][1000 genomes]
rs73600709	0.94[ASN][1000 genomes]
rs73600733	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73600740	0.83[ASN][1000 genomes]
rs74029358	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8046900	0.86[AMR][1000 genomes]
rs8048305	0.95[AMR][1000 genomes]
rs8049910	0.94[ASN][1000 genomes]
rs8053337	0.83[ASN][1000 genomes]
rs8054497	0.94[ASN][1000 genomes]
rs8057181	0.82[ASN][1000 genomes]
rs8063026	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8064052	0.86[AMR][1000 genomes]
rs9921872	0.94[ASN][1000 genomes]
rs9933207	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9933660	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907012	chr16:81986896-82115148	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1058368	chr16:82029516-82152788	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	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

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82045400-82049600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr16:82045600-82049400	Weak transcription	Stomach Mucosa	stomach
3	chr16:82045800-82048400	Weak transcription	Duodenum Smooth Muscle	Duodenum

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