Variant report

Variant	rs35618526
Chromosome Location	chr19:36066044-36066045
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11084824	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11670252	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12610264	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62109963	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62109968	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62109992	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][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	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 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	chr19:36060400-36066400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr19:36060600-36066400	Weak transcription	Spleen	Spleen
3	chr19:36061800-36066400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr19:36062000-36066400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:36062200-36066400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr19:36062600-36066400	Weak transcription	Pancreas	Pancrea
7	chr19:36064800-36066400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr19:36064800-36066400	Weak transcription	Liver	Liver
9	chr19:36065200-36066400	Weak transcription	Right Atrium	heart
10	chr19:36065400-36066400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr19:36065800-36066200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr19:36065800-36066200	Weak transcription	HSMMtube	muscle
13	chr19:36066000-36066200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr19:36066000-36066200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:36066000-36066200	Weak transcription	Adipose Nuclei	Adipose
16	chr19:36066000-36066200	Weak transcription	Fetal Intestine Large	intestine
17	chr19:36066000-36066200	Weak transcription	NHLF	lung

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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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