Variant report

Variant	rs7615390
Chromosome Location	chr3:180193022-180193023
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:180191991..180193577-chr3:180195851..180197734,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11915168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16831623	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16831631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16831633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16831686	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1982978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1982980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28849493	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4390924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58475538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58976802	0.81[AFR][1000 genomes]
rs59189320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59259611	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60339377	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6789734	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6800920	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73043798	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73045721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73045782	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73049997	0.89[AFR][1000 genomes]
rs7616161	0.81[AFR][1000 genomes]
rs7618551	0.81[AFR][1000 genomes]
rs7618861	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7628758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7635826	0.81[AFR][1000 genomes]
rs7647297	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7650795	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9756688	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9756767	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9757646	0.85[AMR][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	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1007831	chr3:180162003-180348203	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv536818	chr3:180162003-180348203	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:180187400-180205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr3:180187600-180193800	Weak transcription	HMEC	breast
3	chr3:180187600-180198800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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