Variant report

Variant	rs74118994
Chromosome Location	chr1:166147797-166147798
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10918382	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10918402	0.85[AMR][1000 genomes]
rs12060595	0.85[AMR][1000 genomes]
rs12239225	0.85[AMR][1000 genomes]
rs12239227	0.85[AMR][1000 genomes]
rs1594568	0.85[AMR][1000 genomes]
rs57918730	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs59517017	0.83[AMR][1000 genomes]
rs61339873	0.85[AMR][1000 genomes]
rs6426971	0.85[AMR][1000 genomes]
rs74122007	0.85[AMR][1000 genomes]
rs7556166	0.85[AMR][1000 genomes]
rs9651029	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9651038	0.87[AFR][1000 genomes];0.85[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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv3332610	chr1:166111288-166282689	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166143200-166151400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:166143600-166148200	Weak transcription	Gastric	stomach
3	chr1:166143800-166154200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:166147600-166147800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:166147600-166165800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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