Variant report

Variant	rs73119195
Chromosome Location	chr1:221810158-221810159
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs57966484	1.00[AFR][1000 genomes]
rs58446643	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58995244	1.00[AMR][1000 genomes]
rs61101563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61507809	1.00[AMR][1000 genomes]
rs61692302	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117560	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117561	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117564	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117573	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117575	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73117576	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73121106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73121110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73121111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73121113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73121116	0.90[AFR][1000 genomes]
rs73121119	0.90[AFR][1000 genomes]
rs73121125	0.90[AFR][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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873200	chr1:221644180-221843191	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr1:221806000-221811200	Weak transcription	Fetal Heart	heart
2	chr1:221806200-221813600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:221809200-221811000	Weak transcription	HMEC	breast
4	chr1:221810000-221811200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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