Variant report

Variant	rs4751570
Chromosome Location	chr10:117632759-117632760
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1552068	1.00[YRI][hapmap];0.98[AFR][1000 genomes]
rs17093691	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2620952	0.88[YRI][hapmap];0.97[AFR][1000 genomes]
rs2620953	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2960658	0.94[AFR][1000 genomes]
rs4237489	0.93[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4328148	1.00[YRI][hapmap];0.98[AFR][1000 genomes]
rs4751934	0.88[AFR][1000 genomes]
rs7922443	1.00[AMR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117631000-117632800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:117632000-117633200	Enhancers	Fetal Stomach	stomach
3	chr10:117632200-117632800	Enhancers	Fetal Intestine Small	intestine
4	chr10:117632600-117633800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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