Variant report

Variant	rs538672944
Chromosome Location	chr16:79663155-79663156
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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	esv274911	chr16:79662740-79664106	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79661400-79663400	Enhancers	HMEC	breast
2	chr16:79661600-79663200	Enhancers	NH-A	brain
3	chr16:79661600-79663200	Enhancers	Osteobl	bone
4	chr16:79661800-79663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr16:79661800-79663200	Enhancers	Primary hematopoietic stem cells	blood
6	chr16:79661800-79663200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr16:79661800-79663200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr16:79662000-79663200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr16:79662000-79663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr16:79662000-79663200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr16:79662000-79663200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr16:79662200-79663200	Enhancers	GM12878-XiMat	blood
13	chr16:79662200-79663600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr16:79662400-79663400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr16:79662600-79666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr16:79663000-79665800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr16:79663000-79665800	Weak transcription	NHEK	skin
18	chr16:79663000-79666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:79663000-79666200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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