Variant report

Variant	rs72929019
Chromosome Location	chr1:67695383-67695384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67692800-67702000	Weak transcription	K562	blood
2	chr1:67693200-67695800	Weak transcription	HMEC	breast
3	chr1:67693400-67695600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:67693600-67695600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:67693600-67695800	Weak transcription	NHEK	skin
6	chr1:67693600-67696000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:67695000-67696200	Enhancers	Esophagus	oesophagus

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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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