Variant report

Variant	rs6919722
Chromosome Location	chr6:13868606-13868607
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10949008	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12207817	0.92[EUR][1000 genomes]
rs12529958	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13201631	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2209250	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35139352	0.92[EUR][1000 genomes]
rs4712134	0.95[EUR][1000 genomes]
rs62385894	0.92[AFR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9475717	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9475727	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13864400-13872600	Weak transcription	Placenta	Placenta
2	chr6:13865600-13873200	Weak transcription	Fetal Intestine Small	intestine
3	chr6:13867200-13872600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr6:13867200-13872600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr6:13867800-13869200	Weak transcription	Fetal Brain Male	brain
6	chr6:13868400-13873400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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