Variant report

Variant rs568455
Chromosome Location chr13:91794294-91794295
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:91787600-91795800 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr13:91789400-91795000 Weak transcription Fetal Kidney kidney
3 chr13:91791000-91794600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr13:91791000-91794800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr13:91791600-91795400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr13:91792200-91796600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr13:91792600-91795000 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr13:91793200-91794400 Enhancers Fetal Muscle Leg muscle
9 chr13:91793800-91795200 Enhancers NH-A brain
10 chr13:91794000-91794400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr13:91794200-91794400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr13:91794200-91794400 Enhancers Pancreatic Islets Pancreatic Islet
13 chr13:91794200-91794400 Enhancers Skeletal Muscle Female skeletal muscle
14 chr13:91794200-91795000 Weak transcription Placenta Placenta
15 chr13:91794200-91796400 Weak transcription Aorta Aorta

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