Variant report

Variant	rs73154336
Chromosome Location	chr22:32988620-32988621
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]
rs131047	0.98[EUR][1000 genomes]
rs135583	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs135584	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4820083	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4821076	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73154334	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73154335	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs739104	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32979400-32994200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr22:32981600-32996200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr22:32986800-32989200	Enhancers	Hela-S3	cervix
4	chr22:32987000-32988800	Enhancers	Osteobl	bone
5	chr22:32988000-32989200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr22:32988000-32989400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr22:32988000-32993200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr22:32988600-32989000	Enhancers	Placenta Amnion	Placenta Amnion

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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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