Variant report

Variant	rs6688556
Chromosome Location	chr1:215157471-215157472
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215141800-215162600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:215155800-215157600	Enhancers	NH-A	brain
3	chr1:215155800-215158600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:215157000-215158000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:215157000-215162400	Weak transcription	NHDF-Ad	bronchial
6	chr1:215157400-215157800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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