Variant report

Variant	rs2137913
Chromosome Location	chr10:50166284-50166285
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50162988..50165937-chr10:50166054..50168309,2	MCF-7	breast:
2	chr10:50165630..50167905-chr10:50168201..50170600,3	K562	blood:
3	chr10:50163078..50165646-chr10:50166132..50168999,2	MCF-7	breast:
4	chr10:50166004..50168125-chr10:50171240..50172846,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1015717	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10745290	0.89[EUR][1000 genomes]
rs10776658	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10776659	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10776660	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10857430	0.89[EUR][1000 genomes]
rs10857431	0.82[EUR][1000 genomes]
rs10857661	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10857662	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11101572	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11101573	0.97[EUR][1000 genomes]
rs12413832	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1877799	0.91[EUR][1000 genomes]
rs1913516	0.89[EUR][1000 genomes]
rs1913526	0.81[EUR][1000 genomes]
rs2137909	0.91[EUR][1000 genomes]
rs2249662	0.82[EUR][1000 genomes]
rs2255553	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2271565	0.92[EUR][1000 genomes]
rs2292584	0.91[EUR][1000 genomes]
rs2292585	0.91[EUR][1000 genomes]
rs2457466	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2663028	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2663067	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2663068	0.82[ASN][1000 genomes]
rs2671715	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2889709	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3750867	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3829206	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4317902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4614357	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4838663	0.91[EUR][1000 genomes]
rs61848117	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6537586	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6537587	0.89[EUR][1000 genomes]
rs7072344	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7082322	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7083751	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7086917	0.89[EUR][1000 genomes]
rs7091429	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7093656	0.89[EUR][1000 genomes]
rs7098224	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7913932	0.82[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50144600-50196200	Strong transcription	Primary B cells from cord blood	blood
2	chr10:50145000-50193200	Strong transcription	Primary B cells from peripheral blood	blood
3	chr10:50145400-50193200	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr10:50145800-50193400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr10:50148000-50193600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:50153400-50187800	Strong transcription	GM12878-XiMat	blood
7	chr10:50153600-50193600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr10:50161200-50167200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr10:50161600-50177800	Weak transcription	Lung	lung
10	chr10:50163200-50173000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr10:50163400-50168000	Strong transcription	Spleen	Spleen
12	chr10:50163400-50189000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:50164200-50170400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:50164400-50166800	Weak transcription	Fetal Muscle Leg	muscle
15	chr10:50165200-50166400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:50166200-50167800	Weak transcription	Primary T cells from cord blood	blood

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