Variant report

Variant	rs9493273
Chromosome Location	chr6:132599386-132599387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132596600-132600800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:132596600-132600800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr6:132596800-132600800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:132596800-132600800	Weak transcription	Fetal Muscle Leg	muscle
5	chr6:132597000-132600800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:132597000-132600800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:132597000-132600800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr6:132597000-132600800	Weak transcription	Fetal Intestine Large	intestine
9	chr6:132597000-132600800	Weak transcription	Stomach Mucosa	stomach
10	chr6:132597400-132600800	Weak transcription	Fetal Intestine Small	intestine
11	chr6:132599000-132600800	Weak transcription	Fetal Brain Female	brain
12	chr6:132599200-132599400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:132599200-132600800	Weak transcription	Fetal Brain Male	brain

Quick Search:

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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