Variant report

Variant	rs13297278
Chromosome Location	chr9:103431809-103431810
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]
rs10989188	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10989190	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10989192	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10989195	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10989208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11791916	1.00[LWK][hapmap]
rs11793359	1.00[LWK][hapmap]
rs12376476	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12376930	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs13298723	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs34268339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34283191	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35510855	0.87[ASN][1000 genomes]
rs55646994	0.87[ASN][1000 genomes]
rs7858958	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103428000-103432000	Weak transcription	Right Atrium	heart
2	chr9:103429800-103432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:103430600-103433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:103431000-103432600	Weak transcription	Fetal Brain Female	brain
5	chr9:103431400-103434800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr9:103431800-103432200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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