Variant report

Variant	rs73779009
Chromosome Location	chr6:132594443-132594444
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	chr6:132589600-132595800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:132590000-132595400	Weak transcription	Aorta	Aorta
3	chr6:132592400-132596000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:132592600-132595400	Weak transcription	Fetal Intestine Large	intestine
5	chr6:132592600-132595400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:132592600-132595600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:132592600-132595800	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:132592600-132596400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:132592800-132595400	Weak transcription	Stomach Mucosa	stomach
10	chr6:132594000-132595800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:132594200-132599200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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