Variant report

Variant	rs9323545
Chromosome Location	chr14:71161277-71161278
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]
rs10144432	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10150936	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11158876	0.83[ASN][1000 genomes]
rs11844559	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12590136	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17108384	0.90[ASN][1000 genomes]
rs7144585	0.87[ASN][1000 genomes]
rs9323546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71133200-71173000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:71143000-71177800	Weak transcription	Primary B cells from cord blood	blood
3	chr14:71153400-71165200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr14:71154400-71165000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr14:71154600-71165000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:71154600-71165200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:71157600-71162400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr14:71160000-71162800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr14:71160200-71163800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr14:71160200-71164600	Weak transcription	Placenta	Placenta

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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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