Variant report

Variant	rs10125809
Chromosome Location	chr9:104389426-104389427
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10114871	0.86[AFR][1000 genomes]
rs10117050	0.87[AFR][1000 genomes]
rs10119079	0.87[AFR][1000 genomes]
rs10119283	0.82[AFR][1000 genomes]
rs10120736	0.82[AFR][1000 genomes]
rs10121691	0.82[AFR][1000 genomes]
rs10122077	0.87[AFR][1000 genomes]
rs10123334	0.87[AFR][1000 genomes]
rs10156603	0.87[AFR][1000 genomes]
rs10989575	1.00[AFR][1000 genomes]
rs10989593	0.87[AFR][1000 genomes]
rs11506966	1.00[AFR][1000 genomes]
rs12339890	0.82[AFR][1000 genomes]
rs12340167	1.00[AFR][1000 genomes]
rs12342952	0.87[AFR][1000 genomes]
rs12343034	0.82[AFR][1000 genomes]
rs12343188	1.00[AFR][1000 genomes]
rs12344042	1.00[AFR][1000 genomes]
rs12344841	1.00[AFR][1000 genomes]
rs12346815	1.00[AFR][1000 genomes]
rs28420755	1.00[AFR][1000 genomes]
rs28436645	0.87[AFR][1000 genomes]
rs28456110	0.82[AFR][1000 genomes]
rs28504973	0.86[AFR][1000 genomes]
rs28612816	1.00[AFR][1000 genomes]
rs28621686	1.00[AFR][1000 genomes]
rs28631285	0.82[AFR][1000 genomes]
rs28680751	0.87[AFR][1000 genomes]
rs28687945	1.00[AFR][1000 genomes]
rs28736781	0.87[AFR][1000 genomes]
rs58800610	0.82[AFR][1000 genomes]
rs73496772	1.00[AFR][1000 genomes]
rs73502933	1.00[AFR][1000 genomes]
rs73504933	0.82[AFR][1000 genomes]
rs73504976	0.82[AFR][1000 genomes]
rs73658427	1.00[AFR][1000 genomes]

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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv6642	chr9:104385959-104398737	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104382400-104392200	Weak transcription	Liver	Liver
2	chr9:104387600-104390400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:104387800-104390400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:104388200-104389600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr9:104389000-104390400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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