Variant report

Variant	rs58845756
Chromosome Location	chr15:45547273-45547274
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57753607	1.00[AMR][1000 genomes]
rs58599469	1.00[AMR][1000 genomes]
rs59653817	1.00[AMR][1000 genomes]
rs60484916	1.00[AMR][1000 genomes]
rs7166428	1.00[AMR][1000 genomes]
rs73406368	1.00[AMR][1000 genomes]
rs73406377	1.00[AMR][1000 genomes]
rs74009611	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74009618	1.00[AMR][1000 genomes]
rs74009621	1.00[AMR][1000 genomes]
rs74009623	0.89[AFR][1000 genomes]
rs74009628	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8031001	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	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 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	chr15:45537200-45547400	Weak transcription	Gastric	stomach
2	chr15:45542400-45549600	Weak transcription	Left Ventricle	heart
3	chr15:45544400-45547800	Active TSS	Duodenum Mucosa	Duodenum
4	chr15:45544400-45547800	Active TSS	Fetal Stomach	stomach
5	chr15:45544400-45554600	Weak transcription	Fetal Intestine Small	intestine
6	chr15:45545200-45547600	Weak transcription	Psoas Muscle	Psoas
7	chr15:45545800-45554600	Weak transcription	Fetal Intestine Large	intestine
8	chr15:45546400-45547800	Enhancers	Osteobl	bone
9	chr15:45546400-45556800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr15:45546600-45547600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr15:45546600-45547600	Enhancers	NHDF-Ad	bronchial
12	chr15:45546800-45547400	Enhancers	NHEK	skin
13	chr15:45547000-45547800	Enhancers	Stomach Mucosa	stomach
14	chr15:45547000-45547800	Enhancers	HepG2	liver
15	chr15:45547200-45547400	Enhancers	Aorta	Aorta
16	chr15:45547200-45547600	Enhancers	HSMM	muscle
17	chr15:45547200-45547800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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