Variant report

Variant	rs12273151
Chromosome Location	chr11:120503351-120503352
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10160371	1.00[AMR][1000 genomes]
rs10160449	1.00[AMR][1000 genomes]
rs11217914	1.00[AMR][1000 genomes]
rs12294271	1.00[AMR][1000 genomes]
rs12295742	1.00[AMR][1000 genomes]
rs17124128	1.00[EUR][1000 genomes]
rs4590879	1.00[AMR][1000 genomes]
rs7101638	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7104127	1.00[AMR][1000 genomes]
rs7119262	0.82[AFR][1000 genomes]
rs7932311	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv468881	chr11:120446830-120551100	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv556476	chr11:120446830-120551100	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120484800-120507400	Weak transcription	Right Atrium	heart
2	chr11:120494000-120504600	Weak transcription	Fetal Lung	lung
3	chr11:120498600-120504600	Weak transcription	Spleen	Spleen
4	chr11:120498800-120505000	Weak transcription	Fetal Intestine Large	intestine
5	chr11:120501000-120504400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:120501200-120504600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:120501200-120504800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:120501400-120503400	Weak transcription	GM12878-XiMat	blood
9	chr11:120502800-120504400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:120503000-120504600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:120503200-120506400	Enhancers	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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