Variant report

Variant	rs10939906
Chromosome Location	chr5:50572996-50572997
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10471516	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1501983	0.86[ASN][1000 genomes]
rs6870975	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6871104	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7704175	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7716272	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7721490	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7721930	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9291726	0.88[EUR][1000 genomes];0.92[ASN][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	nsv1020970	chr5:50569183-50657424	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:50567200-50574400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr5:50569200-50574200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:50569800-50574400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr5:50570000-50574200	Weak transcription	hESC Derived CD184+ Endoderm 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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