Variant report

Variant	rs964503
Chromosome Location	chr4:103349213-103349214
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1037999	0.80[JPT][hapmap]
rs1811810	0.80[JPT][hapmap]
rs2045797	0.80[JPT][hapmap];0.81[ASN][1000 genomes]
rs2045798	1.00[ASN][1000 genomes]
rs2903280	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6533013	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6533014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6533015	0.80[JPT][hapmap];0.82[ASN][1000 genomes]
rs964504	0.91[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103337800-103349800	Weak transcription	NHEK	skin
2	chr4:103342400-103350800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:103342600-103350400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:103345000-103350400	Weak transcription	Dnd41	blood
5	chr4:103348200-103350600	Enhancers	Hela-S3	cervix
6	chr4:103348200-103351800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:103348800-103351600	Enhancers	Liver	Liver
8	chr4:103349200-103349400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:103349200-103351600	Weak transcription	HepG2	liver

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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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