Variant report

Variant	rs66570438
Chromosome Location	chr15:39153472-39153473
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:7)

rs_ID	r²[population]
rs12902694	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12913639	1.00[EUR][1000 genomes]
rs35935215	1.00[EUR][1000 genomes]
rs71470576	1.00[EUR][1000 genomes]
rs71470578	1.00[EUR][1000 genomes]
rs71470579	1.00[EUR][1000 genomes]
rs73396158	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046994	chr15:38806163-39239014	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv832975	chr15:39011915-39227590	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1054810	chr15:39019900-39578526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv542359	chr15:39019900-39578526	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1039615	chr15:39118263-39157687	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1046027	chr15:39126735-39159867	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1040746	chr15:39126735-39327690	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv904090	chr15:39138908-39347192	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:39146800-39154400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr15:39151000-39153800	Enhancers	Fetal Intestine Large	intestine
3	chr15:39151600-39154200	Enhancers	Fetal Intestine Small	intestine
4	chr15:39152000-39156400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:39152200-39153600	Enhancers	Ovary	ovary
6	chr15:39152400-39154800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr15:39152600-39153600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:39152600-39154000	Enhancers	Osteobl	bone
9	chr15:39152600-39155200	Enhancers	NHDF-Ad	bronchial
10	chr15:39152600-39155800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:39152800-39153800	Enhancers	HSMM	muscle
12	chr15:39152800-39160800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr15:39153000-39153600	Enhancers	Adipose Nuclei	Adipose
14	chr15:39153000-39156600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr15:39153200-39153600	Weak transcription	NHLF	lung
16	chr15:39153200-39156600	Weak transcription	Placenta	Placenta
17	chr15:39153400-39155600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:39153400-39156400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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