Variant report

Variant	rs7535780
Chromosome Location	chr1:168418373-168418374
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1102317	0.80[AFR][1000 genomes]
rs12031090	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs858098	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs858100	0.90[CHB][hapmap];0.83[JPT][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168409200-168421400	Weak transcription	HepG2	liver
2	chr1:168409200-168421800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:168416400-168419800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:168416400-168421400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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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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