Variant report

Variant	rs72698241
Chromosome Location	chr9:8623784-8623785
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10511505	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1337808	0.95[ASN][1000 genomes]
rs17573565	0.85[EUR][1000 genomes]
rs56158447	0.91[EUR][1000 genomes]
rs72698237	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72698246	0.91[EUR][1000 genomes]
rs72698247	0.84[EUR][1000 genomes]
rs72698258	0.81[EUR][1000 genomes]
rs72698284	0.85[EUR][1000 genomes]
rs72698291	0.81[EUR][1000 genomes]
rs72698297	0.92[EUR][1000 genomes]
rs72700305	0.90[EUR][1000 genomes]
rs72700307	0.90[EUR][1000 genomes]
rs72700314	0.83[EUR][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	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv831504	chr9:8496277-8665773	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv892230	chr9:8569186-8643259	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv892231	chr9:8569186-8659757	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8614400-8627000	Weak transcription	Fetal Lung	lung
2	chr9:8615200-8627200	Weak transcription	Brain Germinal Matrix	brain
3	chr9:8615400-8624000	Weak transcription	Brain Angular Gyrus	brain
4	chr9:8615400-8626600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr9:8615400-8628000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:8615400-8628000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr9:8615400-8632000	Weak transcription	Fetal Brain Male	brain
8	chr9:8615600-8627800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr9:8615600-8629200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr9:8616800-8648000	Weak transcription	Fetal Kidney	kidney
11	chr9:8620800-8628400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr9:8621000-8628000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:8621800-8624800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr9:8621800-8629800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:8622000-8648600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr9:8622800-8628000	Weak transcription	Fetal Heart	heart
17	chr9:8622800-8629400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:8623200-8627600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr9:8623400-8647800	Weak transcription	Primary hematopoietic stem cells	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