Variant report

Variant	rs60716861
Chromosome Location	chr7:147264850-147264851
allele	C/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]
rs60485461	1.00[AMR][1000 genomes]
rs73741405	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73741406	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73741407	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73741412	1.00[AMR][1000 genomes]
rs73744510	1.00[AMR][1000 genomes]
rs73744517	1.00[AMR][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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 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	chr7:147262200-147269000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr7:147262800-147267800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:147264200-147266000	Weak transcription	Fetal Kidney	kidney
4	chr7:147264600-147268600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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