Variant report

Variant	rs7550069
Chromosome Location	chr1:220693933-220693934
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17007839	1.00[ASN][1000 genomes]
rs17007842	1.00[ASN][1000 genomes]
rs17007883	1.00[AFR][1000 genomes]
rs59662327	1.00[AFR][1000 genomes]
rs59902520	1.00[AFR][1000 genomes]
rs6672055	0.86[EUR][1000 genomes]
rs6695068	1.00[ASN][1000 genomes]
rs6696723	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73101842	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7512507	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7518883	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7518985	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7531134	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7545089	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7552147	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7556342	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220691000-220695000	Weak transcription	NHEK	skin

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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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