Variant report

Variant	rs16973185
Chromosome Location	chr15:33896663-33896664
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11072550	1.00[CEU][hapmap]
rs11852941	1.00[CEU][hapmap];0.80[AFR][1000 genomes]
rs11858539	0.90[AMR][1000 genomes]
rs11858976	1.00[MEX][hapmap]
rs12591509	1.00[MEX][hapmap]
rs16957745	1.00[MEX][hapmap]
rs16971146	1.00[CEU][hapmap]
rs4780163	1.00[MEX][hapmap]
rs4780166	1.00[MEX][hapmap]
rs58822275	1.00[AMR][1000 genomes]
rs61121099	0.90[AMR][1000 genomes]
rs8023957	1.00[CEU][hapmap]
rs8032721	1.00[CEU][hapmap]

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	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv34037	chr15:33732616-34049083	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv431382	chr15:33873751-33915088	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2753712	chr15:33894495-33914004	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33858000-33921200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr15:33859200-33923200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr15:33873000-33923400	Weak transcription	Brain Anterior Caudate	brain
4	chr15:33890800-33897200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:33891800-33921800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr15:33892800-33904200	Weak transcription	Fetal Stomach	stomach
7	chr15:33893400-33897600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:33893800-33905200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:33893800-33911800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr15:33894600-33900400	Weak transcription	Psoas Muscle	Psoas
11	chr15:33895200-33897600	Strong transcription	Fetal Muscle Leg	muscle
12	chr15:33895600-33896800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:33895600-33922800	Weak transcription	Aorta	Aorta

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

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