Variant report

Variant	rs4924566
Chromosome Location	chr15:35431566-35431567
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]
rs10162973	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10163166	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12917609	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13380141	0.89[EUR][1000 genomes]
rs1380091	0.89[EUR][1000 genomes]
rs1809254	0.86[EUR][1000 genomes]
rs1971926	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4924550	0.89[EUR][1000 genomes]
rs60151615	0.83[ASN][1000 genomes]
rs6495757	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7163827	0.85[EUR][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	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1052721	chr15:35381487-35437841	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
4	nsv1050526	chr15:35418676-35437841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35426800-35433400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:35429000-35433800	Weak transcription	Fetal Intestine Large	intestine
3	chr15:35429000-35434800	Weak transcription	Ovary	ovary
4	chr15:35429200-35432000	Weak transcription	Fetal Heart	heart
5	chr15:35429400-35433000	Weak transcription	Fetal Intestine Small	intestine
6	chr15:35429400-35433000	Weak transcription	Fetal Lung	lung
7	chr15:35429400-35433000	Weak transcription	Fetal Stomach	stomach
8	chr15:35429600-35434800	Weak transcription	Left Ventricle	heart
9	chr15:35431200-35431600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr15:35431200-35431800	Weak transcription	Esophagus	oesophagus
11	chr15:35431200-35451800	Weak transcription	Aorta	Aorta

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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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