Variant report

Variant	rs10111801
Chromosome Location	chr8:130541030-130541031
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12676467	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs16904089	0.82[JPT][hapmap]
rs16904092	0.82[JPT][hapmap]
rs16904101	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs28435884	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2894474	0.82[JPT][hapmap]
rs56924935	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57770403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73711574	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73711578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7825384	1.00[MEX][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130537000-130542600	ZNF genes & repeats	K562	blood
2	chr8:130539400-130543400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:130539400-130544000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:130539600-130547800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:130540000-130542200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr8:130540200-130541200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr8:130540400-130541400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:130540400-130541800	Genic enhancers	Dnd41	blood
9	chr8:130540600-130541600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:130541000-130542000	Enhancers	GM12878-XiMat	blood

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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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