Variant report

Variant	rs72950202
Chromosome Location	chr3:116113857-116113858
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10511356	0.98[EUR][1000 genomes]
rs11925640	0.84[EUR][1000 genomes]
rs11927240	0.98[EUR][1000 genomes]
rs16824815	0.90[EUR][1000 genomes]
rs17646114	0.81[EUR][1000 genomes]
rs17646126	0.81[EUR][1000 genomes]
rs17646294	0.86[EUR][1000 genomes]
rs17646747	0.84[EUR][1000 genomes]
rs28590146	0.98[EUR][1000 genomes]
rs34419229	0.90[EUR][1000 genomes]
rs41457247	0.98[EUR][1000 genomes]
rs59313401	0.98[EUR][1000 genomes]
rs59428849	0.98[EUR][1000 genomes]
rs60148139	0.98[EUR][1000 genomes]
rs6771542	0.98[EUR][1000 genomes]
rs6782605	0.86[EUR][1000 genomes]
rs72950173	0.90[EUR][1000 genomes]
rs72950188	0.90[EUR][1000 genomes]
rs72950190	0.90[EUR][1000 genomes]
rs72950194	0.90[EUR][1000 genomes]
rs72951910	0.98[EUR][1000 genomes]
rs72951915	0.98[EUR][1000 genomes]
rs72951916	0.95[EUR][1000 genomes]
rs72951935	0.95[EUR][1000 genomes]
rs72951938	0.98[EUR][1000 genomes]
rs7433207	0.98[EUR][1000 genomes]
rs7619749	0.90[EUR][1000 genomes]
rs7630573	0.98[EUR][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	nsv877361	chr3:116017931-116138039	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2757005	chr3:116085678-116121948	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2759170	chr3:116085678-116121948	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116103000-116142000	Weak transcription	Fetal Lung	lung
2	chr3:116108200-116115200	Weak transcription	Brain Anterior Caudate	brain
3	chr3:116108600-116114200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:116109200-116118600	Weak transcription	Colon Smooth Muscle	Colon
5	chr3:116109600-116118400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr3:116111400-116116600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:116112600-116114200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:116112600-116132800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:116113200-116114600	Enhancers	Brain Substantia Nigra	brain
10	chr3:116113400-116114600	Enhancers	Brain Angular Gyrus	brain
11	chr3:116113600-116114000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr3:116113800-116114000	Enhancers	Brain Hippocampus Middle	brain
13	chr3:116113800-116117600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:116113800-116127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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