Variant report

Variant	rs554086452
Chromosome Location	chr14:83292780-83292781
allele	C/T
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	esv3357488	chr14:83291024-83293572	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv3392705	chr14:83291124-83293547	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3322199	chr14:83291499-83292897	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83292600-83293000	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr14:83292600-83293200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:83292600-83293600	Enhancers	H1 Derived Neuronal Progenitor 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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