Variant report

Variant	rs10071476
Chromosome Location	chr5:90936694-90936695
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12186681	0.81[EUR][1000 genomes]
rs1566996	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2202508	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2657819	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2962380	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36016458	0.83[EUR][1000 genomes]
rs4355554	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90934200-90940400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:90936200-90941000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:90936400-90938400	Weak transcription	Fetal Heart	heart
4	chr5:90936400-90939800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:90936600-90937000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:90936600-90938400	Weak transcription	Fetal Lung	lung
7	chr5:90936600-90942800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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