Variant report

Variant	rs12261653
Chromosome Location	chr10:49585569-49585570
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:17)

rs_ID	r²[population]
rs1009477	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11101291	1.00[AMR][1000 genomes]
rs11101297	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11101301	0.85[AMR][1000 genomes]
rs11101303	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11101315	0.85[AMR][1000 genomes]
rs11101316	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11101319	0.90[AFR][1000 genomes]
rs12241466	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12241476	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12244705	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12253926	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12265885	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12266878	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59115521	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60051862	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7100777	0.85[AMR][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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49572200-49585600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:49573400-49588600	Weak transcription	Primary T cells from cord blood	blood
3	chr10:49573600-49591200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:49574000-49585600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:49574200-49589800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr10:49574600-49589800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr10:49574600-49589800	Weak transcription	Left Ventricle	heart
8	chr10:49574800-49589800	Weak transcription	A549	lung
9	chr10:49575200-49588000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:49576600-49589800	Weak transcription	Aorta	Aorta
11	chr10:49577200-49590000	Weak transcription	Ovary	ovary
12	chr10:49582000-49585600	Weak transcription	Brain Angular Gyrus	brain
13	chr10:49585200-49591200	Weak transcription	Fetal Heart	heart
14	chr10:49585400-49585600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:49585400-49585600	Enhancers	Pancreas	Pancrea
16	chr10:49585400-49585600	Enhancers	NHDF-Ad	bronchial
17	chr10:49585400-49585800	Enhancers	Fetal Intestine Large	intestine
18	chr10:49585400-49586400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:49585400-49586400	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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