Variant report

Variant	rs59688630
Chromosome Location	chr2:144531593-144531594
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12995474	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13021341	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6740197	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144528000-144534800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:144528400-144533600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:144529800-144532600	Weak transcription	Fetal Lung	lung
4	chr2:144529800-144535600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:144530200-144535600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:144530600-144532200	Weak transcription	Primary B cells from cord blood	blood

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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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