Variant report

Variant	rs73704214
Chromosome Location	chr8:121087023-121087024
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:9)

rs_ID	r²[population]
rs16892894	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16893456	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16893464	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16893485	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16893520	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60560198	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61424529	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7010834	0.86[AFR][1000 genomes]
rs73704220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv3348294	chr8:121000288-121250984	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121075600-121095800	Weak transcription	Gastric	stomach
2	chr8:121082600-121090800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr8:121085200-121088000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:121085600-121087600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:121085600-121089800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:121086000-121087200	Weak transcription	Ovary	ovary
7	chr8:121086000-121087400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:121086000-121090200	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:121086000-121094400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr8:121086800-121087400	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr8:121087000-121088000	Enhancers	Primary monocytes fromperipheralblood	blood

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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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