Variant report

Variant	rs10226220
Chromosome Location	chr7:3910406-3910407
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10230252	1.00[AMR][1000 genomes]
rs10231172	1.00[AMR][1000 genomes]
rs10231715	1.00[YRI][hapmap]
rs10232161	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10232222	1.00[AMR][1000 genomes]
rs10232460	1.00[AMR][1000 genomes]
rs10232479	1.00[AMR][1000 genomes]
rs10233390	0.95[AFR][1000 genomes]
rs10235415	1.00[AMR][1000 genomes]
rs10236208	1.00[AMR][1000 genomes]
rs10236726	1.00[AMR][1000 genomes]
rs10237072	1.00[AMR][1000 genomes]
rs10237207	1.00[AMR][1000 genomes]
rs10237489	1.00[AMR][1000 genomes]
rs10237769	1.00[AMR][1000 genomes]
rs10238790	1.00[AMR][1000 genomes]
rs10239119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10239349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10239755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10240764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10240770	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10240776	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10244131	1.00[AMR][1000 genomes]
rs10246377	1.00[AMR][1000 genomes]
rs10247342	1.00[AMR][1000 genomes]
rs10248032	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10249486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10249617	1.00[AMR][1000 genomes]
rs10250749	1.00[AMR][1000 genomes]
rs10250969	1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10250990	1.00[AMR][1000 genomes]
rs10251860	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10252145	1.00[AMR][1000 genomes]
rs10254515	1.00[AMR][1000 genomes]
rs10254942	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10259149	1.00[AMR][1000 genomes]
rs10259421	1.00[AMR][1000 genomes]
rs10259908	1.00[AMR][1000 genomes]
rs10260208	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs10260973	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10261101	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10262755	1.00[AMR][1000 genomes]
rs10262756	1.00[AMR][1000 genomes]
rs10264034	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10265265	1.00[AMR][1000 genomes]
rs10269172	1.00[AMR][1000 genomes]
rs10269554	1.00[AMR][1000 genomes]
rs10269925	1.00[AMR][1000 genomes]
rs10271361	1.00[AMR][1000 genomes]
rs10271525	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10274442	1.00[AMR][1000 genomes]
rs10274450	1.00[AMR][1000 genomes]
rs10275943	1.00[AMR][1000 genomes]
rs10277140	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10277615	1.00[AMR][1000 genomes]
rs10277730	1.00[AMR][1000 genomes]
rs10281035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10281383	1.00[AMR][1000 genomes]
rs10282240	1.00[AMR][1000 genomes]
rs10282727	1.00[AMR][1000 genomes]
rs11505318	1.00[AMR][1000 genomes]
rs11505319	1.00[AMR][1000 genomes]
rs11505320	1.00[AMR][1000 genomes]
rs11505321	1.00[AMR][1000 genomes]
rs11505480	1.00[AMR][1000 genomes]
rs11505481	1.00[AMR][1000 genomes]
rs12333365	1.00[AMR][1000 genomes]
rs12333373	1.00[AMR][1000 genomes]
rs12333491	1.00[AMR][1000 genomes]
rs12333534	1.00[AMR][1000 genomes]
rs12333847	1.00[AMR][1000 genomes]
rs12333850	1.00[AMR][1000 genomes]
rs12333854	1.00[AMR][1000 genomes]
rs16871049	1.00[AMR][1000 genomes]
rs28408018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28462157	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28491068	1.00[AMR][1000 genomes]
rs28496653	1.00[AMR][1000 genomes]
rs28507850	1.00[AMR][1000 genomes]
rs28532947	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28541657	1.00[AMR][1000 genomes]
rs28554772	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28558397	1.00[AMR][1000 genomes]
rs28560779	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28563149	1.00[AMR][1000 genomes]
rs28565971	0.95[AFR][1000 genomes]
rs28568652	1.00[AMR][1000 genomes]
rs28570515	1.00[AMR][1000 genomes]
rs28578945	1.00[AMR][1000 genomes]
rs28581916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28587155	1.00[AMR][1000 genomes]
rs28593083	1.00[AMR][1000 genomes]
rs28656287	1.00[AMR][1000 genomes]
rs28656426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28692586	1.00[AMR][1000 genomes]
rs28715920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28753192	1.00[AMR][1000 genomes]
rs28765162	1.00[AMR][1000 genomes]
rs28833830	1.00[AMR][1000 genomes]
rs28839918	1.00[AMR][1000 genomes]
rs28846162	1.00[AMR][1000 genomes]
rs28856279	1.00[AMR][1000 genomes]
rs34758548	1.00[AMR][1000 genomes]
rs56740561	1.00[AMR][1000 genomes]
rs57744825	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57761987	1.00[AMR][1000 genomes]
rs58738480	1.00[AMR][1000 genomes]
rs59292244	1.00[AMR][1000 genomes]
rs59408720	1.00[AMR][1000 genomes]
rs60243310	1.00[AMR][1000 genomes]
rs60409549	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9655002	1.00[AMR][1000 genomes]
rs9655328	1.00[AMR][1000 genomes]
rs9655329	1.00[AMR][1000 genomes]
rs9655341	1.00[AMR][1000 genomes]
rs9655342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv1029406	chr7:3860894-4477095	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv538685	chr7:3860894-4477095	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1026410	chr7:3869104-4383606	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv887336	chr7:3870810-3934909	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv887337	chr7:3886254-3934909	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1019190	chr7:3896634-3943566	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1025497	chr7:3905444-4176032	Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv538686	chr7:3905444-4176032	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	esv2756053	chr7:3910039-3920129	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
13	nsv433014	chr7:3910039-4054769	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3901200-3959600	Weak transcription	Pancreas	Pancrea
2	chr7:3906800-3949000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3909200-3914000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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