Variant report

Variant	rs9487035
Chromosome Location	chr6:109606927-109606928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000233908	TF binding region
ENSG00000238474	Chromatin interaction
ENSG00000203799	Chromatin interaction
ENSG00000233908	Chromatin interaction
ENSG00000219700	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1008083	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1608043	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs55863350	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs61002917	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6568562	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6568565	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6909900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6924768	0.89[AMR][1000 genomes]
rs73512467	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73518692	0.89[AMR][1000 genomes]
rs73762681	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7753882	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7754671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7762891	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7773100	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9480917	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9480925	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487029	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487030	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487044	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487045	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487050	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487056	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487059	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949883	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109587600-109614600	Weak transcription	HepG2	liver
2	chr6:109591600-109615200	Weak transcription	Placenta	Placenta
3	chr6:109605200-109607000	Enhancers	K562	blood
4	chr6:109606000-109607200	Weak transcription	Fetal Kidney	kidney
5	chr6:109606200-109614400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:109606800-109608800	Enhancers	Fetal Intestine Large	intestine

Quick Search:

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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