Variant report

Variant	rs1383111
Chromosome Location	chr12:26286400-26286401
allele	A/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]
rs1545784	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1545785	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2343073	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2620697	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2620700	0.82[AFR][1000 genomes]
rs2729622	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2729625	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2729648	0.92[AFR][1000 genomes]
rs4963957	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7304897	0.92[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26280000-26287800	Weak transcription	Aorta	Aorta
2	chr12:26280400-26286800	Weak transcription	Brain Substantia Nigra	brain
3	chr12:26280600-26287800	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:26280600-26290200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:26281200-26286600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:26281600-26286600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:26281600-26286600	Weak transcription	HMEC	breast
8	chr12:26284000-26287800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:26284200-26288200	Weak transcription	Spleen	Spleen
10	chr12:26286000-26287000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr12:26286400-26286800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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