Variant report

Variant	rs12276426
Chromosome Location	chr11:34852723-34852724
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10160537	1.00[AFR][1000 genomes]
rs11032883	1.00[AFR][1000 genomes]
rs12287782	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12291078	0.98[AFR][1000 genomes]
rs12291565	1.00[AMR][1000 genomes]
rs12291580	0.82[YRI][hapmap]
rs12291699	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1342027	0.89[AFR][1000 genomes]
rs1857065	0.88[AFR][1000 genomes]
rs7948359	0.93[AFR][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	nsv832118	chr11:34743123-34903951	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv832119	chr11:34815528-35009370	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34847200-34858400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:34848200-34854400	Weak transcription	Esophagus	oesophagus
3	chr11:34851400-34853200	Enhancers	K562	blood
4	chr11:34851600-34852800	Enhancers	Fetal Heart	heart
5	chr11:34852000-34853200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:34852000-34858200	Weak transcription	HepG2	liver
7	chr11:34852200-34853000	Enhancers	Fetal Brain Female	brain
8	chr11:34852200-34853600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:34852200-34853600	Enhancers	Fetal Brain Male	brain
10	chr11:34852400-34852800	Enhancers	NHLF	lung
11	chr11:34852600-34854200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:34852600-34858400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	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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