Variant report

Variant	rs6416498
Chromosome Location	chr15:73229332-73229333
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3352103	chr15:73191535-73454001	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73225000-73230800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:73226200-73230800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:73226600-73230000	Weak transcription	Aorta	Aorta
4	chr15:73228000-73229600	Weak transcription	Psoas Muscle	Psoas
5	chr15:73228400-73229800	Weak transcription	Fetal Stomach	stomach
6	chr15:73229200-73229400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr15:73229200-73229800	Enhancers	Fetal Muscle Trunk	muscle

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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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