Variant report

Variant	rs4368826
Chromosome Location	chr6:150665538-150665539
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1112870	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12055585	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1737283	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4479947	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57892381	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58111791	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs583250	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs585801	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs597663	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs599456	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs654694	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6557468	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs656492	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs683810	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6919940	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6940396	0.82[EUR][1000 genomes]
rs9371950	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9397886	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830843	chr6:150517411-150691173	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4368826	ALPK2	trans	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150664400-150665600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:150664800-150667000	Weak transcription	NH-A	brain
3	chr6:150665200-150666400	Weak transcription	HMEC	breast
4	chr6:150665200-150666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:150665200-150666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:150665200-150666600	Weak transcription	Osteobl	bone
7	chr6:150665200-150666800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:150665200-150666800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:150665400-150667000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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