Variant report

Variant	rs17502383
Chromosome Location	chr13:30306277-30306278
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:15)

rs_ID	r²[population]
rs12864238	1.00[LWK][hapmap]
rs12871145	0.80[AMR][1000 genomes]
rs17073799	0.83[AMR][1000 genomes]
rs1831095	0.83[AMR][1000 genomes]
rs34102821	0.83[AMR][1000 genomes]
rs35933222	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4580011	0.88[EUR][1000 genomes]
rs61947179	1.00[AFR][1000 genomes]
rs66982000	0.83[AMR][1000 genomes]
rs67704126	0.83[AMR][1000 genomes]
rs73157108	0.91[AMR][1000 genomes]
rs7324224	0.83[AMR][1000 genomes]
rs7992067	0.83[AMR][1000 genomes]
rs7996713	0.83[AMR][1000 genomes]
rs9579488	1.00[LWK][hapmap]

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	nsv899961	chr13:30226924-30407273	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr13:30305400-30307400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:30305800-30310600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:30306200-30307800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr13:30306200-30307800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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