Variant report

Variant	rs1886137
Chromosome Location	chr1:58327019-58327020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1408137	0.84[AMR][1000 genomes]
rs1886138	0.86[AMR][1000 genomes]
rs4997596	0.83[AMR][1000 genomes]
rs55733745	0.84[AMR][1000 genomes]
rs55757801	0.84[AMR][1000 genomes]
rs56016455	0.84[AMR][1000 genomes]
rs68051884	0.83[AMR][1000 genomes]
rs723714	0.84[AMR][1000 genomes]
rs72666110	0.84[AMR][1000 genomes]
rs72666111	0.84[AMR][1000 genomes]
rs72666112	0.84[AMR][1000 genomes]
rs72666114	0.84[AMR][1000 genomes]
rs72666115	0.83[AMR][1000 genomes]
rs72666118	0.83[AMR][1000 genomes]
rs72666122	0.83[AMR][1000 genomes]
rs72666124	0.86[AMR][1000 genomes]
rs72666127	0.86[AMR][1000 genomes]
rs72666129	0.86[AMR][1000 genomes]
rs72666132	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv829937	chr1:58258288-58406506	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58320800-58330400	Weak transcription	Fetal Brain Male	brain
2	chr1:58325600-58327200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:58326200-58327200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr1:58326400-58327200	Enhancers	NHEK	skin
5	chr1:58326400-58327400	Enhancers	Fetal Intestine Small	intestine
6	chr1:58326600-58327200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:58326800-58330600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:58326800-58332600	Weak transcription	Fetal Intestine Large	intestine

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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