Variant report

Variant	rs74039633
Chromosome Location	chr16:79698043-79698044
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16950971	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16950996	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs74037503	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74039631	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv833295	chr16:79568878-79726768	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv906992	chr16:79649394-79769790	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv833296	chr16:79692236-79889727	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr16:79688200-79698400	Weak transcription	Right Atrium	heart
2	chr16:79691200-79698200	Weak transcription	Fetal Lung	lung
3	chr16:79693400-79698200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr16:79696600-79698600	Enhancers	Esophagus	oesophagus
5	chr16:79696600-79698800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:79696600-79698800	Enhancers	HMEC	breast
7	chr16:79696800-79698600	Enhancers	NHEK	skin
8	chr16:79697000-79698600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr16:79697800-79698400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr16:79697800-79700600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr16:79698000-79698400	Enhancers	Placenta	Placenta
12	chr16:79698000-79698600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:79698000-79698600	Enhancers	Pancreas	Pancrea

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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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