Variant report

Variant	rs1371382
Chromosome Location	chr5:124582424-124582425
allele	C/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:13)

rs_ID	r²[population]
rs11241798	0.96[ASN][1000 genomes]
rs11954918	0.90[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs11956263	0.98[ASN][1000 genomes]
rs1562126	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs17152551	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59115551	0.93[ASN][1000 genomes]
rs59456631	0.93[ASN][1000 genomes]
rs60808478	0.88[ASN][1000 genomes]
rs62373298	0.94[ASN][1000 genomes]
rs62373302	0.95[ASN][1000 genomes]
rs6880511	0.90[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6890859	1.00[ASN][1000 genomes]
rs920388	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[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	nsv882823	chr5:124569471-124639468	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124546600-124585200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:124581400-124588200	Weak transcription	H1 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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