Variant report

Variant	rs16904097
Chromosome Location	chr8:130512147-130512148
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000266387	TF binding region
ENSG00000265219	TF binding region
ENSG00000264680	TF binding region
ENSG00000265513	TF binding region
ENSG00000265687	TF binding region
ENSG00000266096	TF binding region

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130503600-130519600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:130507600-130516400	Weak transcription	Dnd41	blood
3	chr8:130510600-130512200	Strong transcription	K562	blood

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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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