Variant report

Variant	rs7528475
Chromosome Location	chr1:215378573-215378574
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11120504	0.82[CHB][hapmap]
rs11120519	0.80[CEU][hapmap]
rs12038616	0.91[CHB][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12038695	0.91[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12129983	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12740245	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs12753507	0.80[CEU][hapmap];0.81[CHB][hapmap]
rs2027320	0.96[CEU][hapmap];0.81[CHB][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2363563	0.83[CHB][hapmap]
rs7522552	0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7530450	0.88[YRI][hapmap];0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
2	nsv873170	chr1:215367248-215440975	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
3	esv2760086	chr1:215370570-215381265	Enhancers Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215374800-215380000	Weak transcription	Osteobl	bone
2	chr1:215375000-215379600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:215375000-215387200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:215378200-215378600	Strong transcription	NHDF-Ad	bronchial

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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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