Variant report

Variant	rs73533696
Chromosome Location	chr6:113622923-113622924
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1491087	1.00[AMR][1000 genomes]
rs2637522	1.00[AMR][1000 genomes]
rs2637530	1.00[AMR][1000 genomes]
rs2774522	1.00[AMR][1000 genomes]
rs2801417	1.00[AMR][1000 genomes]
rs2801418	1.00[AMR][1000 genomes]
rs2801421	1.00[AMR][1000 genomes]
rs2801432	1.00[AMR][1000 genomes]
rs2801435	1.00[AMR][1000 genomes]
rs2842836	1.00[AMR][1000 genomes]
rs2842839	1.00[AMR][1000 genomes]
rs2842841	1.00[AMR][1000 genomes]
rs2842847	1.00[AMR][1000 genomes]
rs58633564	1.00[AMR][1000 genomes]
rs60327299	1.00[AMR][1000 genomes]
rs73531803	1.00[AMR][1000 genomes]
rs73531810	1.00[AMR][1000 genomes]
rs73531815	1.00[AMR][1000 genomes]
rs73531818	1.00[AMR][1000 genomes]
rs73531821	1.00[AMR][1000 genomes]
rs73531823	1.00[AMR][1000 genomes]
rs73531888	1.00[AMR][1000 genomes]
rs73533613	1.00[AMR][1000 genomes]
rs73533615	1.00[AMR][1000 genomes]
rs73533619	1.00[AMR][1000 genomes]
rs73533634	1.00[AMR][1000 genomes]
rs73535709	1.00[AMR][1000 genomes]
rs73544585	1.00[AMR][1000 genomes]
rs73545870	1.00[AMR][1000 genomes]
rs73545893	1.00[AMR][1000 genomes]
rs73546314	1.00[AMR][1000 genomes]
rs73546326	1.00[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	nsv604518	chr6:113457727-113700723	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv916294	chr6:113518489-113904305	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113621200-113623000	Weak transcription	Osteobl	bone
2	chr6:113622200-113625400	Enhancers	NHDF-Ad	bronchial
3	chr6:113622600-113623200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:113622600-113623600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:113622800-113623000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:113622800-113623200	Enhancers	NHEK	skin
7	chr6:113622800-113623800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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