Variant report

Variant	rs17043393
Chromosome Location	chr1:216871412-216871413
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11117649	0.82[AMR][1000 genomes]
rs12060770	0.88[CEU][hapmap]
rs1339350	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs17043436	1.00[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs17043466	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2066108	1.00[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs2789721	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs2789722	0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs2789732	0.90[CHB][hapmap]
rs2789733	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs2813666	0.87[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs2813670	0.81[EUR][1000 genomes]
rs2813711	1.00[CEU][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes]
rs2820876	0.81[CHB][hapmap]
rs2820882	1.00[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs2999503	1.00[CEU][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs2999504	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs61817046	0.83[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216864000-216873200	Weak transcription	Fetal Heart	heart
2	chr1:216868200-216894000	Weak transcription	Placenta	Placenta

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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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