Variant report

Variant	rs859624
Chromosome Location	chr1:172730829-172730830
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1102722	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1102729	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12119745	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs704843	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs859725	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172729400-172732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:172730200-172731800	Enhancers	HUVEC	blood vessel
3	chr1:172730200-172732000	Enhancers	HMEC	breast
4	chr1:172730400-172731800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:172730400-172731800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:172730600-172731000	Enhancers	HSMM	muscle
7	chr1:172730600-172731000	Enhancers	Osteobl	bone
8	chr1:172730600-172731200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:172730600-172731400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:172730600-172731400	Enhancers	NHEK	skin
11	chr1:172730600-172731600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:172730600-172731800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:172730800-172731800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	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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