Variant report

Variant	rs7183621
Chromosome Location	chr15:79105576-79105577
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11630027	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12905740	0.82[EUR][1000 genomes]
rs1383636	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1564499	0.85[EUR][1000 genomes]
rs1976007	0.82[EUR][1000 genomes]
rs1994017	0.82[EUR][1000 genomes]
rs28542482	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs2904228	0.87[EUR][1000 genomes]
rs3743057	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3971703	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7182809	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8029039	0.94[EUR][1000 genomes]
rs8038189	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8042170	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs922693	0.84[AFR][1000 genomes];1.00[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	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
2	nsv904431	chr15:79006442-79155088	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv33573	chr15:79053484-79293881	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904432	chr15:79066932-79175813	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79104200-79106000	Weak transcription	Fetal Kidney	kidney
2	chr15:79104800-79106000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr15:79104800-79106800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:79104800-79117800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr15:79104800-79117800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr15:79105000-79106800	Weak transcription	Fetal Brain Female	brain
7	chr15:79105000-79108400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:79105000-79110800	Weak transcription	Right Atrium	heart
9	chr15:79105000-79117800	Weak transcription	HSMMtube	muscle
10	chr15:79105000-79118000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:79105200-79106200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:79105200-79110200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:79105200-79118000	Weak transcription	Right Ventricle	heart

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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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