Variant report

Variant	rs16941740
Chromosome Location	chr17:45323142-45323143
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs13306478	0.89[AMR][1000 genomes]
rs16941829	0.96[AMR][1000 genomes]
rs16941863	0.96[AMR][1000 genomes]
rs16941864	0.96[AMR][1000 genomes]
rs2873530	0.96[AMR][1000 genomes]
rs56221506	0.89[AMR][1000 genomes]
rs8078219	0.89[EUR][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	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45314200-45330200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:45318600-45323400	Weak transcription	NHDF-Ad	bronchial
3	chr17:45318600-45328400	Weak transcription	Fetal Heart	heart
4	chr17:45318600-45329600	Weak transcription	Left Ventricle	heart
5	chr17:45318600-45329600	Weak transcription	Right Atrium	heart
6	chr17:45318600-45330600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr17:45318600-45331200	Weak transcription	HSMMtube	muscle
8	chr17:45321400-45324400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr17:45321600-45323800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr17:45321800-45323200	Enhancers	Spleen	Spleen
11	chr17:45321800-45323600	Enhancers	Fetal Stomach	stomach
12	chr17:45321800-45324000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:45322000-45323600	Enhancers	Fetal Muscle Leg	muscle
14	chr17:45322400-45323400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr17:45322400-45329600	Weak transcription	Ovary	ovary
16	chr17:45323000-45330600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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