Variant report

Variant	rs73770714
Chromosome Location	chr6:121057328-121057329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs73770713	1.00[AFR][1000 genomes]
rs73770715	0.93[AFR][1000 genomes]
rs73770716	1.00[AFR][1000 genomes]
rs73770717	1.00[AFR][1000 genomes]
rs73770718	1.00[AFR][1000 genomes]
rs73770719	1.00[AFR][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	esv3366823	chr6:121043302-121064055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121056600-121058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:121056600-121058600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:121056800-121058000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:121056800-121058000	Enhancers	HMEC	breast
5	chr6:121056800-121058800	Enhancers	NHEK	skin

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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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