Variant report

Variant	rs2919736
Chromosome Location	chr11:70967709-70967710
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1372108	0.87[AMR][1000 genomes]
rs17348351	0.82[JPT][hapmap]
rs2919726	0.87[AMR][1000 genomes]
rs2919740	0.87[AMR][1000 genomes]
rs2919742	0.87[AMR][1000 genomes]
rs3020032	1.00[AMR][1000 genomes]
rs3133512	0.82[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048123	chr11:70795222-71231382	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:70966000-70967800	Enhancers	Placenta	Placenta
2	chr11:70966400-70967800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:70966600-70967800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:70967400-70977000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:70967400-70978800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:70967600-70968600	Enhancers	HepG2	liver
7	chr11:70967600-70974400	Weak transcription	Placenta Amnion	Placenta Amnion

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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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