Variant report

Variant	rs12124770
Chromosome Location	chr1:223695573-223695574
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10796478	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11261301	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17162209	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4281321	0.96[ASN][1000 genomes]
rs4402119	0.85[AFR][1000 genomes]
rs4421579	0.93[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6685101	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:4 , 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
4	chr1:223695200-223695600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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