Variant report

Variant	rs10235650
Chromosome Location	chr7:137158740-137158741
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10223988	0.80[CEU][hapmap]
rs10228926	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs10236626	0.95[EUR][1000 genomes]
rs10236885	0.92[EUR][1000 genomes]
rs10249961	0.95[EUR][1000 genomes]
rs10250999	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10257221	1.00[CEU][hapmap];0.89[YRI][hapmap];0.95[EUR][1000 genomes]
rs10264765	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[EUR][1000 genomes]
rs10268873	0.95[EUR][1000 genomes]
rs10268889	0.95[EUR][1000 genomes]
rs10276002	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10480523	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12707360	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13242243	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13247935	0.93[CHB][hapmap]
rs1406088	1.00[CEU][hapmap];0.96[YRI][hapmap];0.94[EUR][1000 genomes]
rs1528096	0.93[CHB][hapmap]
rs1528098	0.93[CHB][hapmap]
rs1528099	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1528100	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1852641	1.00[CEU][hapmap];0.96[YRI][hapmap];0.95[EUR][1000 genomes]
rs2293546	0.87[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs28434741	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28491569	0.94[EUR][1000 genomes]
rs28573283	0.97[EUR][1000 genomes]
rs34395849	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35080869	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35470018	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35481034	0.94[EUR][1000 genomes]
rs36125942	0.95[EUR][1000 genomes]
rs57998109	0.94[ASN][1000 genomes]
rs6467704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6467705	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[EUR][1000 genomes]
rs6467706	1.00[CEU][hapmap];0.96[YRI][hapmap];0.90[EUR][1000 genomes]
rs6467707	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs67112765	0.95[EUR][1000 genomes]
rs68124742	0.97[EUR][1000 genomes]
rs6950579	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs6951059	0.94[EUR][1000 genomes]
rs6971080	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7341469	0.94[EUR][1000 genomes]
rs7341533	0.95[EUR][1000 genomes]
rs73730628	0.90[ASN][1000 genomes]
rs7778455	0.93[CHB][hapmap]
rs7779526	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7788161	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7792957	0.93[CHB][hapmap]
rs7797211	0.93[CHB][hapmap]
rs7800431	0.93[CHB][hapmap]
rs7802865	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7807425	1.00[CEU][hapmap];0.90[YRI][hapmap];0.95[EUR][1000 genomes]
rs9655902	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv520950	chr7:137154572-137167984	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137139800-137165000	Weak transcription	Fetal Brain Female	brain
2	chr7:137147800-137160600	Weak transcription	NH-A	brain
3	chr7:137148000-137160400	Weak transcription	Brain Anterior Caudate	brain
4	chr7:137148200-137161800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:137148400-137160400	Weak transcription	HSMMtube	muscle
6	chr7:137148400-137160800	Weak transcription	HSMM	muscle
7	chr7:137148600-137206400	Weak transcription	Aorta	Aorta
8	chr7:137149600-137160600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:137149600-137161600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:137150800-137160600	Weak transcription	Osteobl	bone
11	chr7:137151200-137160800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:137152000-137159400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:137152000-137179400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:137158400-137159600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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