Variant report

Variant	rs386432
Chromosome Location	chr7:151008079-151008080
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2530461	0.95[ASN][1000 genomes]
rs367656	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs369386	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs369410	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs442033	0.91[ASN][1000 genomes]
rs450471	0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:151001000-151008200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:151002200-151008400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:151002600-151010600	Weak transcription	Right Atrium	heart
4	chr7:151006200-151008400	Weak transcription	Spleen	Spleen
5	chr7:151006600-151010600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:151006800-151008400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr7:151006800-151010000	Weak transcription	Fetal Lung	lung
8	chr7:151006800-151010800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:151006800-151010800	Weak transcription	NHDF-Ad	bronchial
10	chr7:151007000-151010600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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