Variant report

Variant	rs6983752
Chromosome Location	chr8:59149893-59149894
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11786055	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4448263	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59144200-59150400	Weak transcription	Left Ventricle	heart
2	chr8:59146800-59150600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr8:59146800-59151400	Enhancers	Fetal Brain Male	brain
4	chr8:59147400-59161000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:59147600-59150400	Weak transcription	Fetal Brain Female	brain
6	chr8:59148000-59150400	Weak transcription	NHDF-Ad	bronchial
7	chr8:59148400-59150200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:59149600-59150600	Enhancers	Fetal Lung	lung
9	chr8:59149800-59150000	Enhancers	Placenta	Placenta
10	chr8:59149800-59150800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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