Variant report

Variant	rs10947665
Chromosome Location	chr6:37199130-37199131
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs166393	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2055272	0.80[EUR][1000 genomes]
rs2622885	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3778015	0.80[EUR][1000 genomes]
rs3818136	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4714053	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6914506	0.83[EUR][1000 genomes]
rs6924626	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7739827	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7771855	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9357245	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9380656	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37191200-37199800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:37191400-37207400	Weak transcription	Dnd41	blood
3	chr6:37191400-37207600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:37198000-37204200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:37198200-37199600	Weak transcription	K562	blood
6	chr6:37198200-37200000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:37198600-37200600	Weak transcription	Fetal Intestine Large	intestine

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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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