Variant report

Variant	rs7304544
Chromosome Location	chr12:25455197-25455198
allele	C/T
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]
rs11047941	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11047949	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12228660	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4257070	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4379918	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4438136	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4497495	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4644713	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7299741	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7485340	0.81[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25454400-25456200	Enhancers	Placenta	Placenta
2	chr12:25454600-25455600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:25455000-25456200	Weak transcription	H1 BMP4 Derived Trophoblast 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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