Variant report

Variant	rs11881921
Chromosome Location	chr19:42237641-42237642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:42236111..42237645-chr19:42240491..42242785,2	MCF-7	breast:
2	chr19:42231958..42233812-chr19:42235841..42238635,2	MCF-7	breast:
3	chr19:42236787..42239038-chr19:42291310..42293242,2	MCF-7	breast:
4	chr19:42236810..42239386-chr19:42242980..42245122,2	MCF-7	breast:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10403308	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10406899	0.88[ASN][1000 genomes]
rs10408799	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10411488	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10412553	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10414063	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10415317	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10415946	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10417322	0.87[ASN][1000 genomes]
rs10421687	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10425443	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10853754	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11083637	0.86[ASN][1000 genomes]
rs1115885	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11667651	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11672324	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11878239	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11878262	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12973096	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12985771	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1593086	0.87[ASN][1000 genomes]
rs2002926	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2113133	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2113134	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2161625	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3764577	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3764579	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3829668	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4239514	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4802128	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4802129	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4802130	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4803503	0.88[ASN][1000 genomes]
rs4803505	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4803506	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55997514	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7247317	0.80[ASN][1000 genomes]
rs7252828	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7255070	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs748249	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8106723	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs987066	0.88[EUR][1000 genomes];0.94[ASN][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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	esv3425986	chr19:42212540-42259719	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv579615	chr19:42221434-42310388	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr19:42231400-42237800	Weak transcription	Colonic Mucosa	Colon
2	chr19:42234400-42239800	Enhancers	Stomach Mucosa	stomach
3	chr19:42236400-42237800	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr19:42236400-42241800	Enhancers	Fetal Intestine Large	intestine
5	chr19:42237000-42243400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr19:42237400-42241600	Enhancers	Fetal Intestine Small	intestine
7	chr19:42237600-42238400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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