Variant report

Variant	rs10061576
Chromosome Location	chr5:128144559-128144560
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10062700	0.82[ASN][1000 genomes]
rs1019137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1034898	0.82[EUR][1000 genomes]
rs10478821	0.89[EUR][1000 genomes]
rs1390616	0.88[EUR][1000 genomes]
rs17163935	0.85[EUR][1000 genomes]
rs17163938	0.85[EUR][1000 genomes]
rs17616087	0.82[ASN][1000 genomes]
rs2106979	0.82[ASN][1000 genomes]
rs6595861	0.80[EUR][1000 genomes]
rs6867674	0.89[EUR][1000 genomes]
rs6887514	0.82[ASN][1000 genomes]
rs7707591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7730104	0.82[ASN][1000 genomes]
rs9327489	0.89[EUR][1000 genomes]
rs963437	0.82[ASN][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	nsv1023405	chr5:127955360-128190069	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3392548	chr5:128139102-128159002	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:128143600-128151000	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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