Variant report

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1211376	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1360406	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1360407	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1360409	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1431678	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs220986	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2258208	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2424498	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424499	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424500	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424501	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424502	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4815170	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58357425	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61056253	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6106592	0.86[ASN][1000 genomes]
rs73608985	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22986800-22990200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr20:22988200-22989000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr20:22988200-22989000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr20:22988200-22990200	Enhancers	A549	lung
5	chr20:22988400-22989000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr20:22988400-22989200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr20:22988400-22990200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr20:22988400-22993400	Weak transcription	Aorta	Aorta
9	chr20:22988400-22995600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr20:22988600-22989000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr20:22988600-22989000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr20:22988600-22989000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr20:22988600-22989000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr20:22988600-22989000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr20:22988800-22989000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr20:22988800-22989000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr20:22988800-22989000	Enhancers	HMEC	breast
18	chr20:22988800-22989000	Enhancers	HSMMtube	muscle
19	chr20:22988800-22989600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr20:22988800-22990400	Enhancers	NHDF-Ad	bronchial
21	chr20:22988800-22992000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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