Variant report

Variant	rs35831133
Chromosome Location	chr10:21685944-21685945
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs34785359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34891645	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs71491181	1.00[ASN][1000 genomes]
rs985519	1.00[ASN][1000 genomes]
rs985520	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr10:21678200-21692000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:21680200-21687200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr10:21681600-21687800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr10:21683400-21691200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:21683400-21691200	Weak transcription	Right Atrium	heart
6	chr10:21684200-21687200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:21684200-21696000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:21684600-21687800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:21685400-21686800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr10:21685600-21686000	Enhancers	A549	lung
11	chr10:21685600-21686000	Enhancers	Hela-S3	cervix
12	chr10:21685600-21686000	Enhancers	NHEK	skin
13	chr10:21685600-21686600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr10:21685800-21686000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr10:21685800-21686000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr10:21685800-21686000	Enhancers	NH-A	brain
17	chr10:21685800-21686600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr10:21685800-21686600	Enhancers	Fetal Kidney	kidney

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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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