Variant report

Variant	rs73149174
Chromosome Location	chr3:25115463-25115464
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs59663978	1.00[ASN][1000 genomes]
rs62228548	0.96[ASN][1000 genomes]
rs62230269	1.00[ASN][1000 genomes]
rs6773755	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73141440	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73141467	1.00[ASN][1000 genomes]
rs73141468	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73149145	0.85[AFR][1000 genomes]
rs7618700	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618802	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25111400-25115600	Weak transcription	Fetal Lung	lung
2	chr3:25114600-25116400	Enhancers	Fetal Kidney	kidney
3	chr3:25114800-25115800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:25115400-25116200	Enhancers	Foreskin Melanocyte Primary Cells skin03	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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