Variant report

Variant	rs4748981
Chromosome Location	chr10:25061887-25061888
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs4747498	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4747499	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4747500	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4748977	0.80[EUR][1000 genomes]
rs4748978	0.80[EUR][1000 genomes]
rs6482443	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7911992	0.86[EUR][1000 genomes]
rs951857	0.94[EUR][1000 genomes]
rs951859	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs952917	0.94[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25060200-25063000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:25060800-25062000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr10:25061800-25065600	Weak transcription	Fetal Stomach	stomach

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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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