Variant report

Variant	rs10059409
Chromosome Location	chr5:124464984-124464985
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10044704	0.81[AFR][1000 genomes]
rs10061454	0.91[AFR][1000 genomes]
rs1371380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1371381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1550360	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2119005	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2408304	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4836149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6421892	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6873484	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6889068	0.91[AFR][1000 genomes]
rs893713	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327350	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327352	0.91[AFR][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	nsv830475	chr5:124387292-124550256	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv599658	chr5:124459547-124513012	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124456200-124470000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:124456200-124470200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:124456400-124465000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:124461400-124465200	Weak transcription	NHDF-Ad	bronchial
5	chr5:124461400-124468200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:124464800-124465600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:124464800-124465600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:124464800-124465600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:124464800-124465600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:124464800-124465600	Enhancers	HMEC	breast
11	chr5:124464800-124465800	Enhancers	NHEK	skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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