Variant report

Variant	rs35989243
Chromosome Location	chr8:129901170-129901171
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs12541496	0.85[EUR][1000 genomes]
rs12541508	0.81[EUR][1000 genomes]
rs12544343	0.83[EUR][1000 genomes]
rs12544345	0.83[EUR][1000 genomes]
rs12548853	0.81[EUR][1000 genomes]
rs12549424	0.85[EUR][1000 genomes]
rs12549751	0.83[EUR][1000 genomes]
rs13250924	0.87[EUR][1000 genomes]
rs13257555	0.83[EUR][1000 genomes]
rs13269457	0.83[EUR][1000 genomes]
rs13269648	0.83[EUR][1000 genomes]
rs13272774	0.83[EUR][1000 genomes]
rs13273255	0.81[EUR][1000 genomes]
rs13275784	0.85[EUR][1000 genomes]
rs13280887	0.87[EUR][1000 genomes]
rs1519840	1.00[ASN][1000 genomes]
rs1519858	1.00[ASN][1000 genomes]
rs1596125	0.83[EUR][1000 genomes]
rs16903668	1.00[ASN][1000 genomes]
rs16903677	1.00[ASN][1000 genomes]
rs16903682	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028517	0.85[EUR][1000 genomes]
rs34093858	0.83[EUR][1000 genomes]
rs34757177	0.83[EUR][1000 genomes]
rs34825160	0.85[EUR][1000 genomes]
rs35081453	0.85[EUR][1000 genomes]
rs35181074	0.92[EUR][1000 genomes]
rs35296092	0.85[EUR][1000 genomes]
rs35299722	0.87[EUR][1000 genomes]
rs35643497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35697214	0.83[EUR][1000 genomes]
rs35950030	0.90[EUR][1000 genomes]
rs35960460	0.83[EUR][1000 genomes]
rs36040241	0.83[EUR][1000 genomes]
rs36142507	0.83[EUR][1000 genomes]
rs56884764	0.85[EUR][1000 genomes]
rs57630172	0.85[EUR][1000 genomes]
rs58015045	0.83[EUR][1000 genomes]
rs59460028	1.00[ASN][1000 genomes]
rs61025881	0.83[EUR][1000 genomes]
rs61580176	0.83[EUR][1000 genomes]
rs67628488	0.83[EUR][1000 genomes]
rs6994591	1.00[ASN][1000 genomes]
rs7015615	1.00[ASN][1000 genomes]
rs73373832	0.81[EUR][1000 genomes]
rs73385409	0.90[EUR][1000 genomes]
rs73708224	1.00[ASN][1000 genomes]
rs73708238	1.00[ASN][1000 genomes]
rs73708240	1.00[ASN][1000 genomes]
rs756123	1.00[ASN][1000 genomes]
rs7817073	1.00[ASN][1000 genomes]
rs7820704	1.00[ASN][1000 genomes]
rs7821002	1.00[ASN][1000 genomes]
rs7823984	1.00[ASN][1000 genomes]
rs7846441	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129896400-129901200	Weak transcription	NHLF	lung
2	chr8:129896400-129902400	Weak transcription	HSMM	muscle
3	chr8:129896400-129902800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:129896400-129902800	Weak transcription	Osteobl	bone
5	chr8:129896800-129902800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:129896800-129903200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:129898200-129903200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:129899600-129909800	Weak transcription	Dnd41	blood
9	chr8:129900600-129902800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:129900600-129902800	Weak transcription	NHDF-Ad	bronchial
11	chr8:129901000-129901800	Enhancers	Fetal Thymus	thymus

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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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