Variant report

Variant	rs56064213
Chromosome Location	chr6:117746537-117746538
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17574718	0.80[EUR][1000 genomes]
rs35538886	0.90[EUR][1000 genomes]
rs62433103	0.83[AMR][1000 genomes];0.98[EUR][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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117745200-117746800	Active TSS	Muscle Satellite Cultured Cells	--
2	chr6:117745400-117746600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:117745400-117746600	Active TSS	HMEC	breast
4	chr6:117745400-117746600	Weak transcription	Osteobl	bone
5	chr6:117745400-117747000	Weak transcription	A549	lung
6	chr6:117745800-117747600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:117746200-117746800	Enhancers	Fetal Intestine Small	intestine
8	chr6:117746200-117747000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:117746200-117747200	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr6:117746200-117747200	Active TSS	HSMM	muscle
11	chr6:117746200-117747200	Active TSS	HSMMtube	muscle
12	chr6:117746400-117747400	Active TSS	Fetal Intestine Large	intestine

Quick Search:

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

what's new

Quick links