Variant report

Variant	rs571554993
Chromosome Location	chr16:47748327-47748328
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520355	chr16:47424828-48164777	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv525976	chr16:47583872-48035026	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv428657	chr16:47748036-47913816	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47733800-47750200	Weak transcription	Brain Germinal Matrix	brain
2	chr16:47745600-47750800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr16:47746000-47748800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr16:47746200-47748400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:47746200-47748400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr16:47746200-47748400	Enhancers	HMEC	breast
7	chr16:47746400-47748400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr16:47746400-47748400	Enhancers	NHEK	skin
9	chr16:47746600-47748400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr16:47747000-47749800	Weak transcription	Placenta	Placenta
11	chr16:47747400-47755000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr16:47748000-47753800	Weak transcription	Stomach Mucosa	stomach

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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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