Variant report

Variant	rs2210837
Chromosome Location	chr1:221089590-221089591
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10495157	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1335915	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1335916	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1335928	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1414508	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1414517	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1572384	0.80[EUR][1000 genomes]
rs2484708	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2484709	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2484710	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2784246	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2784273	0.80[EUR][1000 genomes]
rs2784283	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2807866	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221080600-221090200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:221087400-221090000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:221087600-221089600	Enhancers	Liver	Liver
4	chr1:221087800-221089800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr1:221089000-221089600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr1:221089000-221096200	Weak transcription	Spleen	Spleen
7	chr1:221089200-221092200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:221089200-221093800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:221089200-221094800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:221089200-221095400	Weak transcription	Fetal Muscle Leg	muscle

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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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