Variant report

Variant	rs8023125
Chromosome Location	chr14:32772495-32772496
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs2208869	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2383310	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4981956	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6571502	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6571507	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7161546	0.82[AMR][1000 genomes]
rs8005191	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8012126	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32765200-32773600	Weak transcription	Pancreas	Pancrea
2	chr14:32768000-32780000	Weak transcription	Psoas Muscle	Psoas
3	chr14:32768200-32773400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:32768600-32776600	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:32769400-32772600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr14:32769800-32777200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:32769800-32780800	Weak transcription	Left Ventricle	heart
8	chr14:32770000-32773200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:32772200-32774000	Enhancers	Liver	Liver
10	chr14:32772400-32774000	Enhancers	Fetal Intestine Small	intestine

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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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