Variant report

Variant	rs73406161
Chromosome Location	chr15:49373559-49373560
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]
rs16962040	1.00[AMR][1000 genomes]
rs16962045	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16962046	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59905446	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61307981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61578756	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61615150	1.00[AMR][1000 genomes]
rs73406139	1.00[AMR][1000 genomes]
rs73406150	1.00[AMR][1000 genomes]
rs73406154	1.00[AMR][1000 genomes]
rs73406155	1.00[AMR][1000 genomes]
rs73406169	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406171	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406174	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406176	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406183	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406184	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406186	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49368600-49374800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr15:49369200-49377800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr15:49371800-49375200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr15:49372200-49381000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:49372400-49374200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:49373200-49374400	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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