Variant report

Variant	rs11821808
Chromosome Location	chr11:75451187-75451188
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	chr11:75445518..75448042-chr11:75450594..75453068,2	MCF-7	breast:

Extended variants
information (count: 121 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10160784	0.88[ASN][1000 genomes]
rs10160802	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1017713	0.88[ASN][1000 genomes]
rs10219339	0.88[ASN][1000 genomes]
rs10793124	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793125	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793126	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793127	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10793128	0.87[EUR][1000 genomes]
rs10793129	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10793130	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10793132	0.85[ASN][1000 genomes]
rs10793133	0.85[ASN][1000 genomes]
rs10899105	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10899109	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10899110	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10899112	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10899113	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10899114	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10899115	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10899116	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10899119	0.88[ASN][1000 genomes]
rs10899120	0.88[ASN][1000 genomes]
rs10899121	0.87[ASN][1000 genomes]
rs10899122	0.87[ASN][1000 genomes]
rs10899123	0.88[ASN][1000 genomes]
rs10899124	0.87[ASN][1000 genomes]
rs10899127	0.87[ASN][1000 genomes]
rs10899128	0.87[ASN][1000 genomes]
rs10899129	0.86[ASN][1000 genomes]
rs10899131	0.85[ASN][1000 genomes]
rs10899132	0.85[ASN][1000 genomes]
rs10899133	0.85[ASN][1000 genomes]
rs10899134	0.85[ASN][1000 genomes]
rs10899135	0.85[ASN][1000 genomes]
rs10899136	0.85[ASN][1000 genomes]
rs10899137	0.85[ASN][1000 genomes]
rs10899138	0.81[ASN][1000 genomes]
rs10899139	0.81[ASN][1000 genomes]
rs10899140	0.81[ASN][1000 genomes]
rs10899141	0.81[ASN][1000 genomes]
rs10899142	0.81[ASN][1000 genomes]
rs10899145	0.81[ASN][1000 genomes]
rs11236507	0.92[ASN][1000 genomes]
rs11236508	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11236509	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11236511	0.94[ASN][1000 genomes]
rs11236514	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236515	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236516	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236517	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11236518	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236519	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11236525	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11236526	0.91[EUR][1000 genomes]
rs11236527	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11236528	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11236530	0.88[ASN][1000 genomes]
rs11236531	0.87[ASN][1000 genomes]
rs11236533	0.88[ASN][1000 genomes]
rs11236534	0.88[ASN][1000 genomes]
rs11236537	0.84[ASN][1000 genomes]
rs11236538	0.85[ASN][1000 genomes]
rs11236539	0.85[ASN][1000 genomes]
rs11236540	0.85[ASN][1000 genomes]
rs11236542	0.85[ASN][1000 genomes]
rs11236543	0.85[ASN][1000 genomes]
rs11236545	0.85[ASN][1000 genomes]
rs11236546	0.85[ASN][1000 genomes]
rs11236549	0.81[ASN][1000 genomes]
rs11236551	0.81[ASN][1000 genomes]
rs11236552	0.81[ASN][1000 genomes]
rs11236553	0.81[ASN][1000 genomes]
rs11236554	0.81[ASN][1000 genomes]
rs11501918	0.87[ASN][1000 genomes]
rs11822903	0.86[ASN][1000 genomes]
rs11823869	0.88[ASN][1000 genomes]
rs12222542	0.88[ASN][1000 genomes]
rs12222995	0.88[ASN][1000 genomes]
rs12224062	0.81[ASN][1000 genomes]
rs12278224	0.81[ASN][1000 genomes]
rs12278257	0.81[ASN][1000 genomes]
rs12285853	0.85[ASN][1000 genomes]
rs1458836	0.86[ASN][1000 genomes]
rs1806895	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2008476	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28802056	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs36016715	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3740849	0.86[ASN][1000 genomes]
rs3740850	0.86[ASN][1000 genomes]
rs499974	0.88[ASN][1000 genomes]
rs531117	0.88[ASN][1000 genomes]
rs559355	0.88[ASN][1000 genomes]
rs57188913	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58340821	0.88[ASN][1000 genomes]
rs58411334	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59913369	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs600518	0.88[ASN][1000 genomes]
rs600626	0.88[ASN][1000 genomes]
rs60677263	0.88[ASN][1000 genomes]
rs643884	0.88[ASN][1000 genomes]
rs644361	0.88[ASN][1000 genomes]
rs6592615	0.81[ASN][1000 genomes]
rs7101806	0.81[ASN][1000 genomes]
rs7106736	0.85[ASN][1000 genomes]
rs7108178	0.81[ASN][1000 genomes]
rs7110517	0.85[ASN][1000 genomes]
rs7118039	0.81[ASN][1000 genomes]
rs7118293	0.87[ASN][1000 genomes]
rs7122123	0.81[ASN][1000 genomes]
rs7126727	0.87[ASN][1000 genomes]
rs7128716	0.85[ASN][1000 genomes]
rs72995678	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72997616	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72997623	0.86[ASN][1000 genomes]
rs7933235	0.81[ASN][1000 genomes]
rs7944950	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7947418	0.81[ASN][1000 genomes]
rs7947512	0.88[ASN][1000 genomes]

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	esv3381903	chr11:75123498-75587233	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
2	nsv897924	chr11:75424546-75678647	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11821808	RP11-535A19.1	cis	Whole Blood	GTEx
rs11821808	DGAT2	cis	Whole Blood	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75445200-75455000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:75446000-75454200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr11:75446000-75454800	Weak transcription	Psoas Muscle	Psoas
4	chr11:75446800-75454800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr11:75448000-75451600	Enhancers	Liver	Liver
6	chr11:75448600-75453200	Weak transcription	Fetal Intestine Small	intestine
7	chr11:75448800-75453800	Weak transcription	Fetal Intestine Large	intestine
8	chr11:75450400-75453800	Weak transcription	HepG2	liver
9	chr11:75451000-75451400	Enhancers	Stomach Mucosa	stomach

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