Variant report

Variant	rs34044149
Chromosome Location	chr5:68139356-68139357
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs34264944	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34845252	0.82[AMR][1000 genomes]
rs35092707	0.87[AMR][1000 genomes]
rs35260480	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35428898	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35666670	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs71622264	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7730743	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68133000-68142800	Weak transcription	Aorta	Aorta
2	chr5:68135400-68139400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:68135400-68143400	Weak transcription	HMEC	breast
4	chr5:68135400-68143600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:68135600-68140000	Weak transcription	NHDF-Ad	bronchial
6	chr5:68136800-68143400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr5:68139200-68139800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:68139200-68140200	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr5:68139200-68140400	Enhancers	HSMM	muscle

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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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