Variant report

Variant	rs6083433
Chromosome Location	chr20:24180931-24180932
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	chr20:24180566..24182316-chr20:24260551..24262639,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs12373871	1.00[ASN][1000 genomes]
rs28778436	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41282312	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41282314	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41282316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55739770	0.93[EUR][1000 genomes]
rs55771985	0.90[EUR][1000 genomes]
rs56104572	0.89[EUR][1000 genomes]
rs59054030	0.89[EUR][1000 genomes]
rs59561448	0.89[EUR][1000 genomes]
rs6049548	0.83[EUR][1000 genomes]
rs6049554	0.86[EUR][1000 genomes]
rs6049555	0.89[EUR][1000 genomes]
rs6049556	0.89[EUR][1000 genomes]
rs6076185	0.83[EUR][1000 genomes]
rs6076190	0.90[EUR][1000 genomes]
rs6076194	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs6076195	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6076200	1.00[ASN][1000 genomes]
rs6076205	0.93[EUR][1000 genomes]
rs6076206	1.00[ASN][1000 genomes]
rs6076214	0.89[EUR][1000 genomes]
rs6076217	0.85[EUR][1000 genomes]
rs6083374	0.83[EUR][1000 genomes]
rs6083375	0.83[EUR][1000 genomes]
rs6083376	0.83[EUR][1000 genomes]
rs6083378	0.83[EUR][1000 genomes]
rs6083379	0.83[EUR][1000 genomes]
rs6083382	0.83[EUR][1000 genomes]
rs6083383	0.83[EUR][1000 genomes]
rs6083384	0.83[EUR][1000 genomes]
rs6083386	0.83[EUR][1000 genomes]
rs6083388	0.90[EUR][1000 genomes]
rs6083390	0.90[EUR][1000 genomes]
rs6083391	0.90[EUR][1000 genomes]
rs6083398	0.90[EUR][1000 genomes]
rs6083400	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs6083404	0.93[EUR][1000 genomes]
rs6083406	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083408	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083409	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083424	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083430	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6083431	1.00[CEU][hapmap]
rs6083432	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083438	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083439	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083440	1.00[ASN][1000 genomes]
rs6083441	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083449	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6083452	0.93[EUR][1000 genomes]
rs6083463	0.89[EUR][1000 genomes]
rs6083464	0.89[EUR][1000 genomes]
rs6083465	0.89[EUR][1000 genomes]
rs6083467	0.89[EUR][1000 genomes]
rs6083473	0.85[EUR][1000 genomes]
rs6083480	0.85[EUR][1000 genomes]
rs6083484	0.81[EUR][1000 genomes]
rs6083486	0.81[EUR][1000 genomes]
rs6083487	0.81[EUR][1000 genomes]
rs6083488	0.81[EUR][1000 genomes]
rs6106813	0.89[EUR][1000 genomes]
rs61442635	1.00[AFR][1000 genomes]
rs73329997	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73333779	0.89[EUR][1000 genomes]
rs73335617	0.89[EUR][1000 genomes]
rs73337581	1.00[ASN][1000 genomes]
rs7354351	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8124184	1.00[AFR][1000 genomes]
rs8124188	1.00[AFR][1000 genomes]
rs962527	0.96[EUR][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	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
2	esv3328348	chr20:24095746-24285830	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv833945	chr20:24163437-24349462	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 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	chr20:24180400-24182400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:24180800-24181600	Weak transcription	Fetal Heart	heart

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