Variant report

Variant	rs35712888
Chromosome Location	chr7:3860691-3860692
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 121 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10085400	0.89[ASN][1000 genomes]
rs10085568	0.89[ASN][1000 genomes]
rs10241703	0.80[ASN][1000 genomes]
rs10242459	0.80[ASN][1000 genomes]
rs10243770	0.80[ASN][1000 genomes]
rs10244636	0.80[ASN][1000 genomes]
rs10246449	0.89[ASN][1000 genomes]
rs10252169	0.89[ASN][1000 genomes]
rs10254099	0.80[ASN][1000 genomes]
rs10256741	0.89[ASN][1000 genomes]
rs10479833	0.98[ASN][1000 genomes]
rs10479834	0.98[ASN][1000 genomes]
rs10480105	0.98[ASN][1000 genomes]
rs10951315	0.84[ASN][1000 genomes]
rs10951322	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10951336	0.98[ASN][1000 genomes]
rs11973090	0.80[ASN][1000 genomes]
rs11976915	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11977993	0.96[ASN][1000 genomes]
rs12531980	0.81[ASN][1000 genomes]
rs12532040	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12532903	0.96[ASN][1000 genomes]
rs12532912	0.96[ASN][1000 genomes]
rs12536445	0.91[ASN][1000 genomes]
rs12536663	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12537696	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12538997	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12540101	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12540220	0.93[ASN][1000 genomes]
rs12690803	0.80[ASN][1000 genomes]
rs12690804	0.80[ASN][1000 genomes]
rs12701219	0.98[ASN][1000 genomes]
rs12701221	0.96[ASN][1000 genomes]
rs12701227	0.93[ASN][1000 genomes]
rs12701229	0.96[ASN][1000 genomes]
rs13221624	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13236653	0.95[ASN][1000 genomes]
rs13236719	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1548612	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1962783	0.87[ASN][1000 genomes]
rs1962784	0.80[ASN][1000 genomes]
rs1962785	0.80[ASN][1000 genomes]
rs2007554	0.80[ASN][1000 genomes]
rs2057919	0.80[ASN][1000 genomes]
rs2057920	0.80[ASN][1000 genomes]
rs2057921	0.80[ASN][1000 genomes]
rs2079377	0.80[ASN][1000 genomes]
rs2079378	0.83[ASN][1000 genomes]
rs2097900	0.95[ASN][1000 genomes]
rs2341959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28491320	0.80[ASN][1000 genomes]
rs2880204	0.98[ASN][1000 genomes]
rs28845270	0.80[ASN][1000 genomes]
rs34614163	0.95[ASN][1000 genomes]
rs34960833	0.95[ASN][1000 genomes]
rs35261333	0.95[ASN][1000 genomes]
rs41873	0.96[ASN][1000 genomes]
rs4431501	0.80[ASN][1000 genomes]
rs6462361	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6462407	0.80[ASN][1000 genomes]
rs6462411	0.80[ASN][1000 genomes]
rs6462412	0.80[ASN][1000 genomes]
rs6462413	0.80[ASN][1000 genomes]
rs67665990	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6944479	0.92[ASN][1000 genomes]
rs6945778	0.88[ASN][1000 genomes]
rs6948552	0.89[ASN][1000 genomes]
rs6952864	0.80[ASN][1000 genomes]
rs6953036	0.98[ASN][1000 genomes]
rs6953282	0.80[ASN][1000 genomes]
rs6953604	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6954370	0.80[ASN][1000 genomes]
rs6956479	0.80[ASN][1000 genomes]
rs6957166	0.89[ASN][1000 genomes]
rs6957676	0.89[ASN][1000 genomes]
rs6958385	0.80[ASN][1000 genomes]
rs6958535	0.80[ASN][1000 genomes]
rs6959835	0.84[ASN][1000 genomes]
rs6961230	0.90[ASN][1000 genomes]
rs6961561	0.80[ASN][1000 genomes]
rs6963058	0.80[ASN][1000 genomes]
rs6963674	0.80[ASN][1000 genomes]
rs6966030	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968148	0.80[ASN][1000 genomes]
rs6968267	0.80[ASN][1000 genomes]
rs6968272	0.80[ASN][1000 genomes]
rs6968444	0.80[ASN][1000 genomes]
rs6968948	0.80[ASN][1000 genomes]
rs6969052	0.88[ASN][1000 genomes]
rs6969235	0.89[ASN][1000 genomes]
rs6970116	0.80[ASN][1000 genomes]
rs6971639	0.80[ASN][1000 genomes]
rs6971803	0.80[ASN][1000 genomes]
rs6971953	0.80[ASN][1000 genomes]
rs6972806	0.80[ASN][1000 genomes]
rs6973944	0.82[ASN][1000 genomes]
rs6975313	0.82[ASN][1000 genomes]
rs6975723	0.82[ASN][1000 genomes]
rs6977844	0.80[ASN][1000 genomes]
rs6978060	0.80[ASN][1000 genomes]
rs6978318	0.80[ASN][1000 genomes]
rs6978964	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6979937	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6980085	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7778705	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7788747	0.88[ASN][1000 genomes]
rs7794504	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7806494	0.95[ASN][1000 genomes]
rs7807003	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7811839	0.96[ASN][1000 genomes]
rs917198	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9655343	0.80[ASN][1000 genomes]
rs985186	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1021443	chr7:3705273-3889334	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1027624	chr7:3808366-3923408	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv538684	chr7:3808366-3923408	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3848400-3882000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:3849400-3880600	Weak transcription	Aorta	Aorta
3	chr7:3859800-3861000	Enhancers	Pancreas	Pancrea
4	chr7:3860400-3861000	Enhancers	Fetal Muscle Leg	muscle

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