Variant report

Variant	rs4133048
Chromosome Location	chr18:8895530-8895531
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1108112	1.00[AFR][1000 genomes]
rs17408774	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17486397	1.00[AFR][1000 genomes]
rs4420597	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4797335	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4797336	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4797337	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4797338	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4797349	1.00[AFR][1000 genomes]
rs4798694	1.00[AFR][1000 genomes]
rs4798695	1.00[AFR][1000 genomes]
rs4798698	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs4798699	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4798702	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4798711	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4798712	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4798713	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4798714	1.00[EUR][1000 genomes]
rs4798715	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064883	chr18:8709670-9133224	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv833584	chr18:8728616-8904213	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8891800-8896000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr18:8891800-8896000	Weak transcription	HMEC	breast
3	chr18:8891800-8903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr18:8894000-8896800	Enhancers	NHDF-Ad	bronchial
5	chr18:8894400-8896600	Enhancers	NHLF	lung
6	chr18:8895000-8895600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr18:8895000-8896000	Weak transcription	Osteobl	bone
8	chr18:8895000-8896200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr18:8895000-8896400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr18:8895200-8896000	Weak transcription	HSMMtube	muscle
11	chr18:8895200-8896400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr18:8895400-8895800	Weak transcription	K562	blood

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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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