Variant report

Variant	rs62306072
Chromosome Location	chr4:100881158-100881159
allele	G/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	chr4:100872600-100881800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:100872600-100886000	Weak transcription	Primary T cells from cord blood	blood
3	chr4:100872600-100886000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr4:100872600-100886200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr4:100877400-100885400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:100880400-100889600	Weak transcription	Foreskin Fibroblast 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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