Variant report

Variant	rs265257
Chromosome Location	chr2:182245115-182245116
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16867397	1.00[EUR][1000 genomes]
rs265255	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs265260	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55836284	1.00[EUR][1000 genomes]
rs61040384	1.00[EUR][1000 genomes]
rs73027486	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	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1002647	chr2:182078521-182392273	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536064	chr2:182078521-182392273	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
5	nsv834476	chr2:182179249-182360259	Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182237600-182248400	Weak transcription	Primary T cells from cord blood	blood
2	chr2:182237800-182249600	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr2:182238000-182258200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr2:182240000-182247400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:182240000-182257400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:182240200-182245400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr2:182240200-182245400	Weak transcription	Adipose Nuclei	Adipose
8	chr2:182241400-182245400	Weak transcription	Pancreas	Pancrea
9	chr2:182241400-182245400	Weak transcription	NHDF-Ad	bronchial
10	chr2:182241600-182245400	Weak transcription	Dnd41	blood
11	chr2:182241600-182258200	Weak transcription	Fetal Thymus	thymus
12	chr2:182245000-182246000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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