Variant report

Variant	rs1187790
Chromosome Location	chr1:213470675-213470676
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:213462923..213464591-chr1:213470126..213472246,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11120125	1.00[ASN][1000 genomes]
rs11801377	1.00[ASN][1000 genomes]
rs1187798	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1187799	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1187800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1187803	0.89[AFR][1000 genomes]
rs1187806	0.81[AFR][1000 genomes]
rs12127112	1.00[ASN][1000 genomes]
rs1369215	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1656004	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2359570	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2654910	0.83[AFR][1000 genomes]
rs2654912	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2654913	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2817982	1.00[ASN][1000 genomes]
rs2841421	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2841429	1.00[ASN][1000 genomes]
rs2841438	1.00[ASN][1000 genomes]
rs320429	1.00[ASN][1000 genomes]
rs35281247	1.00[ASN][1000 genomes]
rs57318993	1.00[ASN][1000 genomes]
rs58141535	1.00[ASN][1000 genomes]
rs58305443	1.00[ASN][1000 genomes]
rs58489960	1.00[ASN][1000 genomes]
rs58860460	1.00[ASN][1000 genomes]
rs59165361	1.00[ASN][1000 genomes]
rs59319827	1.00[ASN][1000 genomes]
rs60414722	1.00[ASN][1000 genomes]
rs74142114	1.00[ASN][1000 genomes]
rs74142116	1.00[ASN][1000 genomes]
rs74142117	1.00[ASN][1000 genomes]
rs7533253	1.00[CHB][hapmap];1.00[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	esv3392967	chr1:213271844-213490132	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213466600-213476400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr1:213467000-213476200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr1:213469200-213471200	Enhancers	Brain Germinal Matrix	brain
4	chr1:213470200-213470800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:213470400-213470800	ZNF genes & repeats	HSMMtube	muscle
6	chr1:213470600-213470800	Enhancers	K562	blood
7	chr1:213470600-213476400	Weak transcription	HSMM	muscle

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