Variant report

Variant	rs4716014
Chromosome Location	chr6:15966036-15966037
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1342739	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1891515	1.00[AMR][1000 genomes]
rs4716015	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9296995	1.00[EUR][1000 genomes]
rs9464845	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15963000-15966200	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:15963200-15969000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:15963200-15969000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr6:15963600-15968400	Weak transcription	HMEC	breast
5	chr6:15963600-15969000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:15965200-15968600	Weak transcription	K562	blood
7	chr6:15965800-15967200	Enhancers	Fetal Stomach	stomach
8	chr6:15966000-15967200	Enhancers	Stomach Smooth Muscle	stomach
9	chr6:15966000-15971200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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