Variant report

Variant	rs73108782
Chromosome Location	chr20:23987546-23987547
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:23979873..23982563-chr20:23986456..23988446,2	MCF-7	breast:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs2379298	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2379299	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2379300	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28376354	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28433532	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28447541	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28451540	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28516591	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28575651	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28702491	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28718074	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28730969	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843775	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843776	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843777	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4336010	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4390824	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4390830	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4499504	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4499505	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4625985	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56170158	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs56199073	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036606	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036607	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036608	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036609	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036610	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036611	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036612	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6049300	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049301	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049302	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049303	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049304	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049305	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049306	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049307	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049308	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049309	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049310	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049311	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049312	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049313	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049315	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049316	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049317	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049318	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049319	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049321	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049322	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049323	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049324	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049325	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049327	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6049328	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67943254	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68050039	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7261741	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73110738	0.88[EUR][1000 genomes]
rs73110741	0.81[EUR][1000 genomes]
rs8124201	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8124208	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8125708	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9967908	0.94[EUR][1000 genomes];1.00[ASN][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	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833944	chr20:23806288-24021865	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1063474	chr20:23918394-24048069	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1056491	chr20:23955040-24105080	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv18738	chr20:23956042-23994680	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23983800-23991600	Weak transcription	Fetal Kidney	kidney
2	chr20:23984000-23989200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr20:23985800-23992000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:23987000-23988200	Enhancers	Adipose Nuclei	Adipose
5	chr20:23987400-23987800	Enhancers	Right Atrium	heart
6	chr20:23987400-23988000	Enhancers	Fetal Muscle Leg	muscle
7	chr20:23987400-23988800	Enhancers	Fetal Heart	heart

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