Variant report

Variant	rs28647449
Chromosome Location	chr4:30807499-30807500
allele	C/T
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]
rs10012692	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10023716	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28420961	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28489673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28629963	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28720058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9291551	0.81[AFR][1000 genomes]
rs9654124	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9993447	1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30791600-30809800	Weak transcription	Fetal Lung	lung
2	chr4:30795800-30824000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:30796000-30810400	Weak transcription	Fetal Heart	heart
4	chr4:30801200-30809600	Weak transcription	Fetal Stomach	stomach
5	chr4:30803800-30817200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:30804800-30819400	Weak transcription	Aorta	Aorta

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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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