Variant report

Variant	rs7068899
Chromosome Location	chr10:26638885-26638886
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10508719	1.00[EUR][1000 genomes]
rs10829010	1.00[EUR][1000 genomes]
rs12261655	1.00[EUR][1000 genomes]
rs12261938	1.00[EUR][1000 genomes]
rs12267406	1.00[EUR][1000 genomes]
rs7067572	1.00[EUR][1000 genomes]
rs73594355	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr10:26638200-26639000	Enhancers	Stomach Mucosa	stomach
2	chr10:26638800-26643800	Weak transcription	Placenta	Placenta
3	chr10:26638800-26644600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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