Variant report

Variant	rs4838491
Chromosome Location	chr10:50494883-50494884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50492010..50493881-chr10:50494510..50496404,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1001338	1.00[ASN][1000 genomes]
rs1004871	0.92[ASN][1000 genomes]
rs10745254	0.84[ASN][1000 genomes]
rs10776548	0.84[ASN][1000 genomes]
rs10857462	0.80[AFR][1000 genomes]
rs11101077	1.00[ASN][1000 genomes]
rs11812365	0.84[ASN][1000 genomes]
rs11814573	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11816487	1.00[ASN][1000 genomes]
rs11817954	1.00[ASN][1000 genomes]
rs12764079	0.84[ASN][1000 genomes]
rs17009639	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17176642	1.00[ASN][1000 genomes]
rs17176649	1.00[ASN][1000 genomes]
rs17176677	1.00[ASN][1000 genomes]
rs17774672	0.87[ASN][1000 genomes]
rs17783271	1.00[ASN][1000 genomes]
rs2377968	1.00[ASN][1000 genomes]
rs2377970	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377971	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377972	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28728361	0.92[ASN][1000 genomes]
rs2889804	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35852229	0.84[ASN][1000 genomes]
rs4409751	1.00[ASN][1000 genomes]
rs4440951	1.00[ASN][1000 genomes]
rs4838379	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4838484	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4838490	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4838495	0.82[ASN][1000 genomes]
rs6537521	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537522	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7893248	0.86[AFR][1000 genomes]
rs7898878	0.92[ASN][1000 genomes]
rs7900404	0.83[ASN][1000 genomes]
rs7900538	0.87[ASN][1000 genomes]
rs7904928	0.87[ASN][1000 genomes]
rs7906537	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7914160	0.84[ASN][1000 genomes]
rs7919151	0.98[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895376	chr10:50480164-50557211	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50485800-50495000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:50491000-50495800	Weak transcription	Spleen	Spleen
3	chr10:50491200-50496200	Weak transcription	Right Atrium	heart
4	chr10:50491600-50496400	Weak transcription	K562	blood
5	chr10:50491800-50495800	Weak transcription	Left Ventricle	heart
6	chr10:50491800-50496200	Weak transcription	Psoas Muscle	Psoas
7	chr10:50491800-50498800	Weak transcription	Right Ventricle	heart
8	chr10:50492200-50496000	Weak transcription	Fetal Heart	heart
9	chr10:50494200-50495200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr10:50494200-50498000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr10:50494200-50499000	Enhancers	Fetal Muscle Leg	muscle
12	chr10:50494400-50495200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr10:50494400-50495600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr10:50494600-50495200	Enhancers	Primary hematopoietic stem cells	blood
15	chr10:50494600-50496400	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr10:50494600-50496400	Enhancers	Fetal Muscle Trunk	muscle
17	chr10:50494800-50496000	Enhancers	Brain Germinal Matrix	brain

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