Variant report

Variant	rs9386583
Chromosome Location	chr6:107146620-107146621
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12205298	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12206866	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12206870	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12214701	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1970594	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2748289	0.93[EUR][1000 genomes]
rs2748290	0.93[EUR][1000 genomes]
rs9372141	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9373893	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9373894	0.89[EUR][1000 genomes]
rs9384631	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9386584	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9386585	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9386587	0.89[EUR][1000 genomes]
rs9398104	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9398107	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9400053	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9400055	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9400056	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9400057	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:107136000-107148200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:107141200-107148200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:107142000-107147600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr6:107142600-107148200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:107142600-107157400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:107142800-107148200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:107143200-107147200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr6:107146000-107147400	Enhancers	Pancreas	Pancrea
9	chr6:107146200-107147400	Weak transcription	Primary B cells from cord blood	blood
10	chr6:107146400-107149200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr6:107146600-107147000	Weak transcription	Primary B cells from peripheral blood	blood

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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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