Variant report

Variant	rs72718708
Chromosome Location	chr1:85291063-85291064
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85264000-85295600	Weak transcription	NHEK	skin
2	chr1:85282400-85295800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:85287600-85295800	Weak transcription	Right Atrium	heart
4	chr1:85288800-85296800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:85289000-85291800	Enhancers	Fetal Heart	heart
6	chr1:85289400-85330800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:85289800-85291600	Enhancers	Left Ventricle	heart
8	chr1:85290200-85294200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:85291000-85291200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:85291000-85296000	Weak transcription	Right Ventricle	heart
11	chr1:85291000-85300000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	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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