Variant report

Variant	rs2033492
Chromosome Location	chr19:44313596-44313597
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10407794	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs189445	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2195980	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs239947	0.81[AMR][1000 genomes]
rs34424221	0.93[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs349026	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs349027	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs349031	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs349035	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs349036	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs349037	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs349054	0.93[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs349056	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs364691	0.80[ASN][1000 genomes]
rs365785	0.83[ASN][1000 genomes]
rs7251009	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7258953	0.85[AMR][1000 genomes];0.94[ASN][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	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44310200-44314200	Enhancers	HMEC	breast
2	chr19:44310400-44313600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr19:44310400-44314000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr19:44311400-44313800	Weak transcription	NHEK	skin
5	chr19:44313400-44313800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	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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