Variant report

Variant	rs2898269
Chromosome Location	chr5:59505493-59505494
allele	A/T
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:8)

rs_ID	r²[population]
rs10434525	1.00[YRI][hapmap]
rs1155796	1.00[YRI][hapmap]
rs11739760	1.00[YRI][hapmap]
rs11741663	1.00[YRI][hapmap]
rs12658881	1.00[YRI][hapmap]
rs1508859	1.00[YRI][hapmap]
rs2961903	1.00[YRI][hapmap]
rs4128924	1.00[YRI][hapmap]

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	nsv1018015	chr5:58889470-59532667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv537766	chr5:58889470-59532667	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59501000-59505800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:59503000-59505600	Enhancers	Fetal Brain Male	brain
3	chr5:59503200-59506600	Weak transcription	HepG2	liver
4	chr5:59503800-59506000	Enhancers	HUVEC	blood vessel
5	chr5:59504000-59506600	Weak transcription	Primary B cells from cord blood	blood
6	chr5:59504200-59505600	Enhancers	Adipose Nuclei	Adipose
7	chr5:59504400-59505600	Enhancers	Fetal Brain Female	brain
8	chr5:59504600-59506000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:59504800-59506600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:59504800-59506800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:59505000-59505800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr5:59505000-59506000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr5:59505200-59505600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:59505200-59505800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr5:59505200-59506000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:59505400-59505800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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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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