Variant report

Variant	rs10276660
Chromosome Location	chr7:96362400-96362401
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10226466	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10234669	0.91[EUR][1000 genomes]
rs10236162	0.87[EUR][1000 genomes]
rs10242066	0.95[EUR][1000 genomes]
rs10246774	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10249910	0.87[EUR][1000 genomes]
rs10252396	1.00[EUR][1000 genomes]
rs10259875	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10270175	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10270486	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10273237	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10278521	0.91[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1581538	0.95[EUR][1000 genomes]
rs1608739	0.95[EUR][1000 genomes]
rs17167680	0.87[EUR][1000 genomes]
rs17167699	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17413240	0.93[EUR][1000 genomes]
rs17495340	0.86[EUR][1000 genomes]
rs1917482	0.95[EUR][1000 genomes]
rs2140741	0.95[EUR][1000 genomes]
rs2272	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3942589	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55902035	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67368115	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67548673	1.00[EUR][1000 genomes]
rs67658953	0.95[EUR][1000 genomes]
rs73228327	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73228328	0.95[EUR][1000 genomes]
rs73228329	0.95[EUR][1000 genomes]
rs73228347	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73228355	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73228356	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73228360	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73228364	0.93[EUR][1000 genomes]
rs7341440	1.00[EUR][1000 genomes]
rs952005	0.86[AMR][1000 genomes];1.00[EUR][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	nsv532174	chr7:96221237-96375826	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv831065	chr7:96275832-96436031	Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96351400-96372800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:96359600-96363600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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