Variant report

Variant	rs10989206
Chromosome Location	chr9:103432198-103432199
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10217205	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10283519	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10283522	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10989209	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10989210	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36196957	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4454339	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4554530	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4742787	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4742790	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4743405	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4743411	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4743412	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62577640	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7851200	0.80[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103429800-103432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:103430600-103433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:103431000-103432600	Weak transcription	Fetal Brain Female	brain
4	chr9:103431400-103434800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr9:103431800-103432200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:103432000-103432400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr9:103432000-103432400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr9:103432000-103433000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr9:103432000-103434000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr9:103432000-103434600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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