Variant report

Variant	rs262358
Chromosome Location	chr7:103462106-103462107
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10234631	1.00[EUR][1000 genomes]
rs10244228	1.00[EUR][1000 genomes]
rs10248650	1.00[EUR][1000 genomes]
rs12112270	1.00[EUR][1000 genomes]
rs12112464	1.00[EUR][1000 genomes]
rs262371	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6965019	1.00[EUR][1000 genomes]
rs73405640	1.00[EUR][1000 genomes]
rs73405671	1.00[EUR][1000 genomes]
rs73405677	1.00[EUR][1000 genomes]
rs73715928	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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv523031	chr7:103457789-103470499	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 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	chr7:103457800-103472000	Weak transcription	HepG2	liver
2	chr7:103461200-103482400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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