Variant report

Variant	rs7203695
Chromosome Location	chr16:48232536-48232537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10163354	1.00[ASN][1000 genomes]
rs10163462	0.84[CEU][hapmap];1.00[ASN][1000 genomes]
rs10221107	1.00[GIH][hapmap]
rs11076565	1.00[GIH][hapmap]
rs11552148	1.00[GIH][hapmap]
rs11861031	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs11861127	0.84[ASN][1000 genomes]
rs11863133	0.93[ASN][1000 genomes]
rs11863233	0.93[ASN][1000 genomes]
rs11863236	0.93[ASN][1000 genomes]
rs11863325	1.00[ASN][1000 genomes]
rs11866251	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs11866312	0.93[ASN][1000 genomes]
rs11866529	1.00[GIH][hapmap];0.93[ASN][1000 genomes]
rs13336264	0.86[ASN][1000 genomes]
rs16945916	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs16945917	1.00[ASN][1000 genomes]
rs16945919	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs16945972	0.93[ASN][1000 genomes]
rs16945974	0.85[ASN][1000 genomes]
rs17743256	1.00[ASN][1000 genomes]
rs28376623	0.93[ASN][1000 genomes]
rs28503414	0.93[ASN][1000 genomes]
rs28605399	0.85[ASN][1000 genomes]
rs28617382	1.00[GIH][hapmap]
rs28626252	0.93[ASN][1000 genomes]
rs28654935	0.93[ASN][1000 genomes]
rs28684834	0.93[ASN][1000 genomes]
rs28696036	0.93[ASN][1000 genomes]
rs41280939	1.00[ASN][1000 genomes]
rs5017203	0.93[ASN][1000 genomes]
rs57912486	1.00[ASN][1000 genomes]
rs62058521	1.00[ASN][1000 genomes]
rs62058522	1.00[ASN][1000 genomes]
rs62058526	1.00[ASN][1000 genomes]
rs62058528	1.00[ASN][1000 genomes]
rs6500339	0.92[ASN][1000 genomes]
rs6500385	1.00[GIH][hapmap]
rs7184831	1.00[ASN][1000 genomes]
rs7187233	1.00[ASN][1000 genomes]
rs7191844	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs7206909	1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs73540901	0.93[ASN][1000 genomes]
rs73542903	0.93[ASN][1000 genomes]
rs73542904	0.93[ASN][1000 genomes]
rs73546434	0.85[ASN][1000 genomes]
rs73546437	0.85[ASN][1000 genomes]
rs73546439	0.85[ASN][1000 genomes]
rs74018298	0.92[ASN][1000 genomes]
rs74018300	1.00[ASN][1000 genomes]
rs8046408	1.00[GIH][hapmap]
rs8046814	0.93[ASN][1000 genomes]
rs8047091	1.00[GIH][hapmap];0.93[ASN][1000 genomes]
rs8047397	0.85[ASN][1000 genomes]
rs8050120	0.84[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8051016	0.87[GIH][hapmap];0.93[ASN][1000 genomes]
rs8051205	1.00[GIH][hapmap];0.93[ASN][1000 genomes]
rs8051441	1.00[GIH][hapmap]
rs8054314	1.00[GIH][hapmap]
rs8055028	1.00[GIH][hapmap]
rs8055128	0.85[ASN][1000 genomes]
rs8056100	0.85[ASN][1000 genomes]
rs8056143	0.85[ASN][1000 genomes]
rs8057475	0.93[ASN][1000 genomes]
rs8060696	0.85[ASN][1000 genomes]
rs8060722	0.85[ASN][1000 genomes]
rs8190	1.00[GIH][hapmap]
rs9302758	1.00[GIH][hapmap]
rs957881	1.00[ASN][1000 genomes]
rs9925772	1.00[GIH][hapmap]
rs9932850	0.93[ASN][1000 genomes]
rs9940038	1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059259	chr16:48113396-48304404	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv542916	chr16:48113396-48304404	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48230200-48240400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr16:48231000-48235400	Weak transcription	HepG2	liver

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