Variant report

Variant	rs73058248
Chromosome Location	chr1:185871435-185871436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10127552	1.00[AFR][1000 genomes]
rs12239000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28507443	0.91[AFR][1000 genomes]
rs28571005	0.91[AFR][1000 genomes]
rs41317459	1.00[AFR][1000 genomes]
rs57642813	1.00[AFR][1000 genomes]
rs57646071	0.91[AFR][1000 genomes]
rs57647869	0.97[AFR][1000 genomes]
rs61492840	0.91[AFR][1000 genomes]
rs6675790	1.00[AFR][1000 genomes]
rs6686746	0.89[AFR][1000 genomes]
rs6689317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6701269	0.89[AFR][1000 genomes]
rs6701921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6703750	0.91[AFR][1000 genomes]
rs73054405	0.97[AFR][1000 genomes]
rs73054410	0.97[AFR][1000 genomes]
rs73054419	1.00[AFR][1000 genomes]
rs73054444	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73054452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73054473	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73058244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73058365	0.80[AFR][1000 genomes]
rs73058381	0.91[AFR][1000 genomes]
rs73058389	0.86[AFR][1000 genomes]
rs73060472	0.91[AFR][1000 genomes]
rs73060496	0.91[AFR][1000 genomes]
rs73062176	1.00[AMR][1000 genomes]
rs73062507	0.91[AFR][1000 genomes]
rs73070566	0.91[AFR][1000 genomes]
rs73070580	0.91[AFR][1000 genomes]
rs73070588	0.86[AFR][1000 genomes]
rs73070592	0.91[AFR][1000 genomes]
rs73070595	0.91[AFR][1000 genomes]
rs73072044	0.91[AFR][1000 genomes]
rs73072053	0.91[AFR][1000 genomes]
rs73072054	0.91[AFR][1000 genomes]
rs73072072	0.97[AFR][1000 genomes]
rs73072073	0.97[AFR][1000 genomes]
rs9727715	0.91[AFR][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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185867000-185872400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:185868000-185878400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links