Variant report

Variant	rs6964339
Chromosome Location	chr7:105225091-105225092
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105222000-105229800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:105222200-105229800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:105222200-105253000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:105222400-105225400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:105222800-105237000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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