Variant report

Variant	rs17270875
Chromosome Location	chr2:182216681-182216682
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16867400	1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16867401	1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16867402	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16867405	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16867406	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16867413	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17198619	0.81[EUR][1000 genomes]
rs55812282	0.81[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:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182208000-182226400	Weak transcription	Fetal Thymus	thymus
2	chr2:182215600-182217600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:182215800-182217600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:182215800-182217600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr2:182215800-182217800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr2:182216000-182217600	Enhancers	Primary B cells from cord blood	blood
7	chr2:182216000-182217800	Enhancers	Primary B cells from peripheral blood	blood
8	chr2:182216000-182217800	Enhancers	Primary hematopoietic stem cells	blood
9	chr2:182216000-182217800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:182216400-182216800	Enhancers	Primary T cells from cord blood	blood
11	chr2:182216400-182217400	Enhancers	Dnd41	blood
12	chr2:182216600-182217200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:182216600-182217600	Enhancers	GM12878-XiMat	blood

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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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