Variant report

Variant	rs10163746
Chromosome Location	chr18:24356523-24356524
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs7229182	0.94[AFR][1000 genomes]
rs8095788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761995	chr18:24214286-24502570	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24351800-24360400	Weak transcription	Dnd41	blood
2	chr18:24354000-24356600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr18:24355200-24358000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr18:24355400-24356600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr18:24355400-24356600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr18:24355600-24357200	Weak transcription	HMEC	breast
7	chr18:24355800-24357200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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