Variant report

Variant	rs72719401
Chromosome Location	chr1:84457525-84457526
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84446200-84461800	Weak transcription	Aorta	Aorta
2	chr1:84451200-84461000	Weak transcription	Gastric	stomach
3	chr1:84451200-84464000	Weak transcription	Pancreas	Pancrea
4	chr1:84451400-84462200	Weak transcription	Stomach Mucosa	stomach
5	chr1:84452600-84459000	Weak transcription	Brain Angular Gyrus	brain
6	chr1:84452600-84460000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:84452600-84462200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:84452600-84462200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr1:84452600-84464000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:84453400-84462400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:84454000-84464000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:84454800-84459000	Weak transcription	Brain Substantia Nigra	brain
13	chr1:84454800-84460000	Weak transcription	HSMM	muscle
14	chr1:84455600-84462200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr1:84455800-84459000	Weak transcription	Brain Hippocampus Middle	brain
16	chr1:84457200-84459800	Weak transcription	Brain Anterior Caudate	brain

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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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