Variant report

Variant	rs61114547
Chromosome Location	chr11:85268708-85268709
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1046216	0.86[ASN][1000 genomes]
rs11600919	0.86[ASN][1000 genomes]
rs11603256	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11606688	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11821005	0.91[ASN][1000 genomes]
rs1213257	0.83[ASN][1000 genomes]
rs1847433	0.87[ASN][1000 genomes]
rs2081445	0.85[ASN][1000 genomes]
rs2840343	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs290183	0.84[ASN][1000 genomes]
rs290184	0.86[ASN][1000 genomes]
rs3753050	0.87[ASN][1000 genomes]
rs3781815	0.86[ASN][1000 genomes]
rs3817087	0.88[ASN][1000 genomes]
rs3824956	0.87[ASN][1000 genomes]
rs3862782	0.85[ASN][1000 genomes]
rs4015271	0.81[ASN][1000 genomes]
rs4301809	0.95[ASN][1000 genomes]
rs4943922	0.83[ASN][1000 genomes]
rs4944523	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4944526	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4944530	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs522604	0.91[ASN][1000 genomes]
rs552013	0.91[ASN][1000 genomes]
rs55841425	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56738052	0.84[AFR][1000 genomes]
rs57245119	0.84[ASN][1000 genomes]
rs57296431	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57549298	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs592460	0.91[ASN][1000 genomes]
rs61342895	0.92[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs61567739	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7107788	0.87[ASN][1000 genomes]
rs7113528	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7116195	0.83[ASN][1000 genomes]
rs7122887	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7925739	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7940714	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7949567	0.87[ASN][1000 genomes]
rs881120	0.91[ASN][1000 genomes]
rs956202	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv898046	chr11:85180409-85300458	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv898047	chr11:85180409-85377707	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
9	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv898049	chr11:85231475-85292310	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	esv3463542	chr11:85262872-85274882	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3463553	chr11:85262901-85274878	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	esv3463564	chr11:85262929-85274858	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
15	esv3463575	chr11:85263028-85274777	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv2421768	chr11:85263724-85271345	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv2829954	chr11:85263724-85271345	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
18	nsv555630	chr11:85263724-85271345	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv32962	chr11:85264773-85272684	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
20	nsv555631	chr11:85266321-85271345	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs61114547	SYTL2	cis	Muscle Skeletal	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85248800-85292000	Weak transcription	Aorta	Aorta
2	chr11:85261400-85284000	Weak transcription	Left Ventricle	heart
3	chr11:85268600-85269400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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