Variant report

Variant	rs545812452
Chromosome Location	chr8:49809575-49809576
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv890854	chr8:49738821-49838908	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3377959	chr8:49809299-49813497	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49802000-49814800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr8:49804200-49811200	Weak transcription	Fetal Kidney	kidney
3	chr8:49804600-49811400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:49804800-49811600	Weak transcription	HMEC	breast
5	chr8:49805000-49811400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:49805600-49811400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:49805600-49811600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:49805800-49810600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:49807200-49811800	Weak transcription	NHDF-Ad	bronchial
10	chr8:49807600-49812000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:49808800-49809800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:49808800-49818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:49809400-49809600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr8:49809400-49809800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr8:49809400-49809800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:49809400-49810200	Enhancers	Hela-S3	cervix
17	chr8:49809400-49817800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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