Variant report

Variant	rs73421718
Chromosome Location	chr9:14996966-14996967
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs55707542	1.00[AMR][1000 genomes]
rs58304447	1.00[AMR][1000 genomes]
rs60560774	1.00[AMR][1000 genomes]
rs73421735	1.00[AFR][1000 genomes]
rs73421742	0.94[AFR][1000 genomes]
rs73421748	1.00[AFR][1000 genomes]
rs73642460	1.00[AMR][1000 genomes]
rs73642465	1.00[AMR][1000 genomes]
rs73642466	1.00[AMR][1000 genomes]
rs73642467	1.00[AMR][1000 genomes]
rs73642468	1.00[AMR][1000 genomes]
rs73642481	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2761503	chr9:14960217-15049343	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv892622	chr9:14960217-15055607	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14993800-15002400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:14994400-15002400	Weak transcription	Brain Anterior Caudate	brain
3	chr9:14994400-15020000	Weak transcription	Brain Angular Gyrus	brain
4	chr9:14994600-15011200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr9:14994800-15020000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:14995000-14999400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr9:14995000-15000000	Weak transcription	HUVEC	blood vessel
8	chr9:14995000-15004000	Weak transcription	Fetal Muscle Leg	muscle
9	chr9:14995200-15000000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:14995600-14997600	Weak transcription	Dnd41	blood

Quick Search:

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

what's new

Quick links