Variant report

Variant	rs9889104
Chromosome Location	chr16:48147280-48147281
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13335175	1.00[AMR][1000 genomes]
rs13336441	1.00[AMR][1000 genomes]
rs13336832	1.00[AMR][1000 genomes]
rs28361908	1.00[AMR][1000 genomes]
rs28379458	1.00[AMR][1000 genomes]
rs28539217	1.00[AMR][1000 genomes]
rs28661941	1.00[AMR][1000 genomes]
rs28848294	1.00[AMR][1000 genomes]
rs9922477	1.00[AMR][1000 genomes]
rs9926437	1.00[AMR][1000 genomes]
rs9928527	1.00[AMR][1000 genomes]
rs9929780	1.00[AMR][1000 genomes]
rs9931267	1.00[AMR][1000 genomes]
rs9931866	1.00[AMR][1000 genomes]
rs9932677	1.00[AMR][1000 genomes]
rs9934175	1.00[AMR][1000 genomes]
rs9934918	1.00[AMR][1000 genomes]
rs9936494	1.00[AMR][1000 genomes]
rs9938115	1.00[AMR][1000 genomes]
rs9938350	1.00[AMR][1000 genomes]
rs9938594	1.00[AMR][1000 genomes]
rs9940237	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520355	chr16:47424828-48164777	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1059259	chr16:48113396-48304404	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv542916	chr16:48113396-48304404	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48139200-48151000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:48144800-48150600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:48146000-48147600	Enhancers	Fetal Muscle Leg	muscle
4	chr16:48146400-48147400	Enhancers	Brain Germinal Matrix	brain
5	chr16:48146400-48160600	Weak transcription	Right Atrium	heart
6	chr16:48146600-48147600	Enhancers	Psoas Muscle	Psoas
7	chr16:48146600-48147800	Enhancers	Fetal Heart	heart
8	chr16:48146600-48147800	Enhancers	Right Ventricle	heart
9	chr16:48146800-48147400	Enhancers	Pancreas	Pancrea
10	chr16:48146800-48147400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr16:48147000-48148000	Enhancers	Left Ventricle	heart
12	chr16:48147000-48148000	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr16:48147200-48147400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr16:48147200-48147800	Enhancers	Fetal Muscle Trunk	muscle

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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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