Variant report

Variant	rs61846637
Chromosome Location	chr10:50781498-50781499
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	chr10:50780517..50784653-chr10:50786786..50789571,3	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1130028	0.86[EUR][1000 genomes]
rs11812473	0.84[EUR][1000 genomes]
rs11815156	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11819019	0.86[EUR][1000 genomes]
rs17010079	0.84[EUR][1000 genomes]
rs17719092	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17775180	0.87[EUR][1000 genomes]
rs2228526	0.87[EUR][1000 genomes]
rs2228527	0.87[EUR][1000 genomes]
rs2228529	0.86[EUR][1000 genomes]
rs36079558	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4253011	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4253028	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4253042	0.89[EUR][1000 genomes]
rs4253049	0.89[EUR][1000 genomes]
rs4253055	0.89[EUR][1000 genomes]
rs4253101	0.87[EUR][1000 genomes]
rs4253106	0.87[EUR][1000 genomes]
rs4253121	0.87[EUR][1000 genomes]
rs4253165	0.87[EUR][1000 genomes]
rs4253166	0.87[EUR][1000 genomes]
rs4253193	0.87[EUR][1000 genomes]
rs56164647	0.86[EUR][1000 genomes]
rs58002245	0.87[EUR][1000 genomes]
rs58711755	0.89[EUR][1000 genomes]
rs58912975	0.84[EUR][1000 genomes]
rs59898389	0.89[EUR][1000 genomes]
rs61846612	0.89[EUR][1000 genomes]
rs61846615	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61846616	0.90[EUR][1000 genomes]
rs61846617	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61846618	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61846620	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61850971	0.84[EUR][1000 genomes]
rs61850976	0.85[EUR][1000 genomes]
rs7067651	0.81[EUR][1000 genomes]
rs7073830	0.87[EUR][1000 genomes]
rs7093098	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7097122	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7097866	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7909222	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7920256	0.87[EUR][1000 genomes]
rs971667	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv831867	chr10:50607857-50788751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50778000-50782600	Enhancers	Hela-S3	cervix
2	chr10:50779000-50782000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:50779400-50782200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr10:50779400-50782400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:50779400-50782400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr10:50780000-50787400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:50780200-50782200	Enhancers	Placenta	Placenta
8	chr10:50780600-50782200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr10:50781000-50781600	Active TSS	HepG2	liver
10	chr10:50781200-50792000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr10:50781400-50782200	Enhancers	Osteobl	bone

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