Variant report

Variant	rs17056045
Chromosome Location	chr6:128902045-128902046
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1281245	1.00[CEU][hapmap]
rs1281246	1.00[CEU][hapmap]
rs1341586	1.00[EUR][1000 genomes]
rs17055961	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17055964	1.00[EUR][1000 genomes]
rs17055978	1.00[EUR][1000 genomes]
rs17055990	1.00[EUR][1000 genomes]
rs17056023	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs17056025	1.00[YRI][hapmap]
rs17056041	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17056084	1.00[EUR][1000 genomes]
rs17056088	1.00[EUR][1000 genomes]
rs17056165	1.00[CEU][hapmap]
rs59615501	1.00[EUR][1000 genomes]
rs6569534	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs73591395	1.00[EUR][1000 genomes]
rs73772055	1.00[EUR][1000 genomes]
rs73772058	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128901600-128902200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:128901800-128902200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:128902000-128903000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:128902000-128903200	Weak transcription	H1 BMP4 Derived Trophoblast 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