Variant report

Variant	rs73123067
Chromosome Location	chr7:63363220-63363221
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:63362448..63365939-chr7:63385089..63387223,4	MCF-7	breast:
2	chr7:63360688..63363246-chr7:63384808..63387419,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265017	Chromatin interaction
ENSG00000227910	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10227601	0.88[EUR][1000 genomes]
rs10238234	0.87[EUR][1000 genomes]
rs10245110	0.87[EUR][1000 genomes]
rs11978874	0.87[EUR][1000 genomes]
rs17138355	0.87[EUR][1000 genomes]
rs17138416	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17840380	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2033829	0.87[EUR][1000 genomes]
rs3751565	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4717940	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55723393	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56149388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56229596	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56249171	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56310951	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56378232	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56381247	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56696237	0.87[EUR][1000 genomes]
rs6460102	0.88[EUR][1000 genomes]
rs66487504	0.88[EUR][1000 genomes]
rs73123042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73123044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73123069	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73123071	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73123077	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73123091	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73123093	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73127180	0.87[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	nsv888255	chr7:63175168-63990100	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
2	nsv888257	chr7:63226279-63464342	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv888258	chr7:63294907-63537173	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv534361	chr7:63328472-63955286	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	nsv966815	chr7:63359141-63370063	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv888259	chr7:63363001-64009193	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:63360800-63365400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr7:63361800-63370800	Weak transcription	Aorta	Aorta
3	chr7:63361800-63372800	Weak transcription	Esophagus	oesophagus
4	chr7:63361800-63379000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:63362000-63366600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:63362200-63364600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:63362200-63372800	Weak transcription	Ovary	ovary
8	chr7:63362200-63376200	Weak transcription	Colon Smooth Muscle	Colon
9	chr7:63362400-63372800	Weak transcription	Brain Anterior Caudate	brain
10	chr7:63362400-63372800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:63362400-63384400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr7:63363200-63364000	ZNF genes & repeats	Dnd41	blood
13	chr7:63363200-63374600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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