Variant report

Variant	rs72985938
Chromosome Location	chr2:209458980-209458981
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs55974317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56199915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56325500	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72985935	0.96[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72985936	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72985950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73987539	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs73987541	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood
2	chr2:209457400-209460000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:209458800-209459000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:209458800-209459000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:209458800-209459400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr2:209458800-209460600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:209458800-209460600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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