Variant report

Variant	rs11050126
Chromosome Location	chr12:29359670-29359671
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs35244320	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73073782	1.00[EUR][1000 genomes]
rs7955386	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532233	chr12:29009388-29496179	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29325400-29364600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:29346000-29360800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr12:29354000-29360400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr12:29357400-29360200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr12:29357800-29360400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:29358000-29362400	Weak transcription	Primary T cells from cord blood	blood
7	chr12:29358200-29361600	Weak transcription	Primary B cells from cord blood	blood
8	chr12:29358400-29362000	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:29359000-29359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr12:29359000-29360600	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr12:29359200-29360200	Weak transcription	Small Intestine	intestine
12	chr12:29359200-29364000	Enhancers	Fetal Intestine Small	intestine
13	chr12:29359200-29366400	Enhancers	Fetal Intestine Large	intestine
14	chr12:29359400-29360000	Enhancers	Brain Hippocampus Middle	brain
15	chr12:29359400-29361400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr12:29359600-29360600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:29359600-29361400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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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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