Variant report

Variant	rs73511912
Chromosome Location	chr6:107151508-107151509
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10485221	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11965826	0.86[EUR][1000 genomes]
rs12111123	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12661223	0.82[EUR][1000 genomes]
rs12665651	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17052232	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17567332	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1977148	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2354224	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28537731	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34702989	0.82[EUR][1000 genomes]
rs35913079	0.82[EUR][1000 genomes]
rs4946777	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4946781	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59742959	1.00[EUR][1000 genomes]
rs60838249	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6914551	0.82[EUR][1000 genomes]
rs6934849	0.82[EUR][1000 genomes]
rs7357000	0.86[EUR][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:107142600-107157400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:107149000-107152800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:107149800-107152000	Enhancers	Stomach Mucosa	stomach
4	chr6:107150000-107152200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr6:107150000-107152400	Enhancers	Pancreas	Pancrea
6	chr6:107151000-107151600	Enhancers	GM12878-XiMat	blood
7	chr6:107151000-107152600	Weak transcription	Esophagus	oesophagus
8	chr6:107151000-107153000	Enhancers	Primary B cells from cord blood	blood
9	chr6:107151000-107154400	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:107151000-107162200	Weak transcription	Fetal Kidney	kidney
11	chr6:107151200-107151600	Active TSS	Liver	Liver
12	chr6:107151200-107151800	Enhancers	HepG2	liver

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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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