Variant report

Variant	rs73604046
Chromosome Location	chr10:28015564-28015565
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs57933197	1.00[AMR][1000 genomes]
rs73604023	1.00[AMR][1000 genomes]
rs73604040	0.86[AFR][1000 genomes]
rs73604048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73604052	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73604053	1.00[AMR][1000 genomes]
rs73604057	1.00[AMR][1000 genomes]
rs73604064	1.00[AMR][1000 genomes]
rs73604066	1.00[AMR][1000 genomes]
rs73604067	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv3368825	chr10:27864181-28043820	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28007200-28016000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:28012400-28016200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr10:28012800-28020000	Weak transcription	Fetal Stomach	stomach
4	chr10:28013400-28016800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:28013400-28016800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:28013400-28020400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:28014000-28017600	Active TSS	Stomach Smooth Muscle	stomach
8	chr10:28014200-28015600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:28014800-28016000	Active TSS	Aorta	Aorta
10	chr10:28015000-28016200	Weak transcription	Colon Smooth Muscle	Colon
11	chr10:28015000-28017400	Active TSS	Ovary	ovary
12	chr10:28015400-28015600	Active TSS	Osteobl	bone
13	chr10:28015400-28017400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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