Variant report

Variant	rs73902578
Chromosome Location	chr20:24043404-24043405
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs28578736	1.00[AMR][1000 genomes]
rs56296104	1.00[AMR][1000 genomes]
rs57302629	1.00[AMR][1000 genomes]
rs57522977	1.00[AMR][1000 genomes]
rs58508170	1.00[AMR][1000 genomes]
rs59273058	1.00[AMR][1000 genomes]
rs59470315	1.00[AMR][1000 genomes]
rs73902532	1.00[AMR][1000 genomes]
rs73902537	1.00[AMR][1000 genomes]
rs73902543	1.00[AMR][1000 genomes]
rs73902551	1.00[AMR][1000 genomes]
rs73902561	1.00[AMR][1000 genomes]
rs73902564	1.00[AMR][1000 genomes]
rs73902570	1.00[AMR][1000 genomes]
rs73902591	1.00[AMR][1000 genomes]
rs8113949	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063474	chr20:23918394-24048069	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1056491	chr20:23955040-24105080	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv962543	chr20:24037279-24044544	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24041800-24046800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr20:24042800-24043600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr20:24043200-24043600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr20:24043400-24045800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr20:24043400-24046200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr20:24043400-24046200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr20:24043400-24046600	Weak transcription	Primary hematopoietic stem cells	blood

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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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