Variant report

Variant	rs61818349
Chromosome Location	chr1:215356122-215356123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs61818070	1.00[AMR][1000 genomes]
rs61818322	1.00[AMR][1000 genomes]
rs61819678	1.00[AMR][1000 genomes]
rs61819679	1.00[AMR][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	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215355000-215356200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:215355000-215356400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:215355000-215356400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:215355000-215356400	ZNF genes & repeats	Gastric	stomach
5	chr1:215355000-215356600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:215355200-215356200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:215355200-215356200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:215355200-215356400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
9	chr1:215356000-215356400	Strong transcription	NHDF-Ad	bronchial
10	chr1:215356000-215356600	Strong transcription	Osteobl	bone
11	chr1:215356000-215360800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:215356000-215364800	Weak transcription	NHLF	lung
13	chr1:215356000-215368400	Weak transcription	Fetal Brain Female	brain

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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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