Variant report

Variant	rs17043379
Chromosome Location	chr2:115468352-115468353
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs13401032	1.00[AMR][1000 genomes]
rs17040472	1.00[AMR][1000 genomes]
rs17043347	1.00[AMR][1000 genomes]
rs17043375	1.00[AMR][1000 genomes]
rs17043382	1.00[AMR][1000 genomes]
rs72955626	1.00[AMR][1000 genomes]
rs72955637	1.00[AMR][1000 genomes]
rs72955641	1.00[AMR][1000 genomes]
rs72955645	1.00[AMR][1000 genomes]
rs72955660	1.00[AMR][1000 genomes]
rs72955672	1.00[AMR][1000 genomes]
rs72955673	1.00[AMR][1000 genomes]
rs72955686	1.00[AMR][1000 genomes]
rs72955695	1.00[AMR][1000 genomes]
rs72955698	1.00[AMR][1000 genomes]
rs72955701	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv431502	chr2:115139566-115617936	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv834338	chr2:115320185-115481229	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv431524	chr2:115425650-115530770	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115465600-115469200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:115466600-115468400	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:115466600-115468600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:115466600-115469200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:115466600-115469200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:115466600-115469600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:115466800-115469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:115467000-115468400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:115467200-115468600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:115467400-115468400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr2:115467800-115469000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:115467800-115471600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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