Variant report

Variant	rs62430580
Chromosome Location	chr6:133382160-133382161
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:133134077..133136797-chr6:133382132..133384671,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112306	Chromatin interaction
ENSG00000206754	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10457002	0.86[EUR][1000 genomes]
rs12192002	0.89[EUR][1000 genomes]
rs12192605	0.89[EUR][1000 genomes]
rs12193118	0.89[EUR][1000 genomes]
rs12198619	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs12199972	0.82[EUR][1000 genomes]
rs12205139	0.94[EUR][1000 genomes]
rs12210093	0.82[EUR][1000 genomes]
rs12212715	0.93[EUR][1000 genomes]
rs28538690	0.83[EUR][1000 genomes]
rs4077767	0.82[EUR][1000 genomes]
rs4257872	0.82[EUR][1000 genomes]
rs4273707	0.85[EUR][1000 genomes]
rs4273708	0.85[EUR][1000 genomes]
rs4895952	0.82[EUR][1000 genomes]
rs57161827	0.89[EUR][1000 genomes]
rs58835706	0.93[EUR][1000 genomes]
rs62430562	0.82[EUR][1000 genomes]
rs62430581	0.98[EUR][1000 genomes]
rs62430582	0.93[EUR][1000 genomes]
rs62430588	0.85[EUR][1000 genomes]
rs62430590	0.85[EUR][1000 genomes]
rs6902225	0.80[EUR][1000 genomes]
rs6902347	0.82[EUR][1000 genomes]
rs6911954	0.86[EUR][1000 genomes]
rs6927627	0.85[EUR][1000 genomes]
rs6933214	0.89[EUR][1000 genomes]
rs6935070	0.85[EUR][1000 genomes]
rs6935480	0.85[EUR][1000 genomes]
rs6936410	0.85[EUR][1000 genomes]
rs6937029	0.84[EUR][1000 genomes]
rs6939899	0.82[EUR][1000 genomes]
rs6940959	0.85[EUR][1000 genomes]
rs72557636	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs7738156	0.85[EUR][1000 genomes]
rs7738592	0.88[EUR][1000 genomes]
rs7754486	0.80[EUR][1000 genomes]
rs7756171	0.83[EUR][1000 genomes]
rs7761372	0.89[EUR][1000 genomes]
rs9321388	0.82[EUR][1000 genomes]
rs9321389	0.82[EUR][1000 genomes]
rs9483529	0.85[EUR][1000 genomes]
rs9483530	0.85[EUR][1000 genomes]
rs9483535	0.82[EUR][1000 genomes]
rs9493513	0.82[EUR][1000 genomes]
rs9493515	0.85[EUR][1000 genomes]
rs9493517	0.85[EUR][1000 genomes]
rs9493518	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv428154	chr6:133271975-133522803	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3445931	chr6:133347824-133434532	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv519475	chr6:133350936-133474673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133376800-133383200	Weak transcription	Fetal Lung	lung
2	chr6:133377000-133383400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:133377200-133384000	Weak transcription	Left Ventricle	heart
4	chr6:133377200-133384000	Weak transcription	Psoas Muscle	Psoas
5	chr6:133378800-133383400	Weak transcription	Brain Anterior Caudate	brain
6	chr6:133382000-133383000	Weak transcription	Fetal Heart	heart

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