Variant report

Variant	rs62337594
Chromosome Location	chr4:160365346-160365347
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160350600-160367800	Weak transcription	HSMM	muscle
2	chr4:160357600-160367000	Weak transcription	NH-A	brain
3	chr4:160362800-160365800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:160362800-160366800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr4:160363800-160365600	Enhancers	NHLF	lung
6	chr4:160364200-160368000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:160364400-160365400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:160364400-160365800	Weak transcription	HMEC	breast
9	chr4:160364400-160367600	Weak transcription	NHEK	skin
10	chr4:160364600-160367400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:160364800-160368000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:160365000-160365600	Enhancers	Fetal Lung	lung

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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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