Variant report

Variant	rs60836137
Chromosome Location	chr12:26234921-26234922
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10842669	0.82[AMR][1000 genomes]
rs11048409	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12368460	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12369397	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12425863	0.83[ASN][1000 genomes]
rs16930076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2048609	0.82[AMR][1000 genomes]
rs2137550	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2620705	0.82[AMR][1000 genomes]
rs2669564	0.83[AMR][1000 genomes]
rs2669565	0.86[AMR][1000 genomes]
rs2669566	0.83[AMR][1000 genomes]
rs2729626	0.86[AMR][1000 genomes]
rs4963952	0.82[AMR][1000 genomes]
rs4963953	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7132288	0.82[AMR][1000 genomes]
rs7306344	0.83[AMR][1000 genomes]
rs73080984	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9804762	0.82[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv976037	chr12:26228360-26244803	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26201600-26236200	Weak transcription	Right Ventricle	heart
2	chr12:26222800-26245800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr12:26229000-26235000	Weak transcription	Aorta	Aorta
4	chr12:26231200-26244200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:26231400-26243800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:26231400-26243800	Weak transcription	NHDF-Ad	bronchial
7	chr12:26231400-26244000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:26231600-26243600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:26234000-26235000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr12:26234000-26235200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr12:26234000-26235200	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr12:26234000-26235400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:26234600-26235200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:26234600-26235200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:26234600-26235200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:26234600-26235200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr12:26234600-26235400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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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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