Variant report

Variant	rs12315893
Chromosome Location	chr12:47220365-47220366
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12317975	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs17097368	1.00[CHB][hapmap]
rs4262792	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs58135862	0.83[EUR][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	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47219800-47220600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
2	chr12:47219800-47221800	Weak transcription	Esophagus	oesophagus
3	chr12:47219800-47224000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr12:47219800-47224200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:47219800-47224200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr12:47219800-47224400	Weak transcription	Right Ventricle	heart
7	chr12:47220000-47220400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr12:47220000-47220400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr12:47220000-47220600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:47220000-47220600	Enhancers	HSMM	muscle
11	chr12:47220000-47224600	Weak transcription	Pancreas	Pancrea
12	chr12:47220200-47220400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr12:47220200-47221200	Enhancers	Liver	Liver
14	chr12:47220200-47221800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:47220200-47224000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr12:47220200-47224200	Weak transcription	NHEK	skin
17	chr12:47220200-47224400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr12:47220200-47224400	Weak transcription	Foreskin Fibroblast 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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