Variant report

Variant	rs10796478
Chromosome Location	chr1:223697236-223697237
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11261301	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12124770	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17162209	0.94[ASN][1000 genomes]
rs4281321	0.91[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4421579	0.94[ASN][1000 genomes]
rs6685101	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223691400-223699600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:223693400-223699600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:223693400-223699600	Weak transcription	Spleen	Spleen

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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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