Variant report

Variant	rs62523765
Chromosome Location	chr8:130645432-130645433
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:17)

rs_ID	r²[population]
rs1077235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57557483	0.85[EUR][1000 genomes]
rs62523762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62523764	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62523766	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62523775	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62523777	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62523778	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62523814	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs62523815	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62523816	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs62523818	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62523819	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs62523821	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62523824	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62523825	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62525621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612230	chr8:130624121-130661901	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130636800-130651600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:130638200-130647600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:130640200-130651600	Weak transcription	Fetal Muscle Leg	muscle
4	chr8:130643600-130646200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:130643800-130646400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:130644800-130646000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr8:130644800-130646000	Enhancers	Brain Substantia Nigra	brain
8	chr8:130645000-130647800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:130645200-130645600	Enhancers	Brain Angular Gyrus	brain
10	chr8:130645200-130645800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:130645200-130645800	Enhancers	Brain Cingulate Gyrus	brain
12	chr8:130645400-130645600	Enhancers	Fetal Brain Male	brain
13	chr8:130645400-130646000	Enhancers	Brain Hippocampus Middle	brain

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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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