Variant report

Variant	rs35013903
Chromosome Location	chr15:60622926-60622927
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1027899	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11071517	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12901654	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12903877	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12903959	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17191358	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17270097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36160486	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67897916	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7169359	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60621600-60627600	Weak transcription	NHDF-Ad	bronchial
2	chr15:60621800-60623200	Weak transcription	HSMM	muscle
3	chr15:60621800-60627600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:60622200-60623800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:60622800-60623200	Weak transcription	Fetal Intestine Small	intestine

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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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