Variant report

Variant	rs12126632
Chromosome Location	chr1:221357227-221357228
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11118653	0.80[ASN][1000 genomes]
rs11118662	0.93[ASN][1000 genomes]
rs11118663	0.97[ASN][1000 genomes]
rs11118664	0.96[ASN][1000 genomes]
rs12120171	0.94[ASN][1000 genomes]
rs12121213	0.88[ASN][1000 genomes]
rs12122167	1.00[ASN][1000 genomes]
rs12123182	0.87[ASN][1000 genomes]
rs12124230	0.93[ASN][1000 genomes]
rs12127195	0.84[ASN][1000 genomes]
rs12128432	0.97[ASN][1000 genomes]
rs12140672	0.91[ASN][1000 genomes]
rs1341619	0.97[ASN][1000 genomes]
rs1442462	0.89[ASN][1000 genomes]
rs1539140	0.97[ASN][1000 genomes]
rs17009529	0.91[ASN][1000 genomes]
rs17009536	0.88[ASN][1000 genomes]
rs17009652	0.85[ASN][1000 genomes]
rs1935157	0.88[ASN][1000 genomes]
rs2039956	0.91[ASN][1000 genomes]
rs3920857	0.88[ASN][1000 genomes]
rs4420085	0.91[ASN][1000 genomes]
rs4427411	0.84[ASN][1000 genomes]
rs4846687	0.82[ASN][1000 genomes]
rs4846690	0.82[ASN][1000 genomes]
rs57489853	0.91[ASN][1000 genomes]
rs59093055	0.84[ASN][1000 genomes]
rs59098418	0.91[ASN][1000 genomes]
rs6670400	0.87[ASN][1000 genomes]
rs6679997	0.89[ASN][1000 genomes]
rs6693821	0.89[ASN][1000 genomes]
rs67635817	0.91[ASN][1000 genomes]
rs7515181	0.90[ASN][1000 genomes]
rs7522767	0.82[ASN][1000 genomes]
rs7522861	0.88[ASN][1000 genomes]
rs7539794	0.97[ASN][1000 genomes]
rs7549116	0.86[ASN][1000 genomes]
rs9431425	0.88[ASN][1000 genomes]
rs9431431	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873199	chr1:221136672-221451217	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221351800-221360800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr1:221355200-221357800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr1:221356200-221357400	Enhancers	Primary hematopoietic stem cells	blood
4	chr1:221356200-221358200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:221356200-221358200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr1:221356800-221360400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:221357000-221357400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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