Variant report

Variant	rs149302454
Chromosome Location	chr8:69951851-69951852
allele	C/T
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	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv33773	chr8:69951243-69952200	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69944000-69953600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr8:69946600-69955400	Weak transcription	Fetal Lung	lung
3	chr8:69951600-69952000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:69951600-69952000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:69951600-69952000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:69951600-69952000	Enhancers	HSMM	muscle
7	chr8:69951600-69952200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:69951600-69952200	Enhancers	NHDF-Ad	bronchial
9	chr8:69951600-69952400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:69951600-69952400	Enhancers	HMEC	breast
11	chr8:69951600-69952400	Enhancers	NHEK	skin
12	chr8:69951600-69952400	Enhancers	Osteobl	bone
13	chr8:69951600-69952600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:69951800-69952600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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