Variant report

Variant	rs17044698
Chromosome Location	chr2:53661851-53661852
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1494018	0.87[ASN][1000 genomes]
rs17044426	1.00[EUR][1000 genomes]
rs17044658	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2131785	0.86[ASN][1000 genomes]
rs2131786	0.86[ASN][1000 genomes]
rs58983989	1.00[EUR][1000 genomes]
rs72909405	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002145	chr2:53387912-53832213	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv535718	chr2:53387912-53832213	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv997401	chr2:53515629-53863347	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv3383918	chr2:53585059-53710179	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv984438	chr2:53649278-53685651	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53659000-53664400	Weak transcription	Hela-S3	cervix
2	chr2:53660400-53663800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:53660600-53663600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:53660600-53663600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:53660600-53664800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr2:53660800-53662600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr2:53661000-53663600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:53661200-53663200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:53661200-53663600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:53661400-53662600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:53661400-53663400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:53661400-53663400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:53661600-53662000	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr2:53661600-53666200	Enhancers	H9 Derived Neuron 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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