Variant report

Variant rs12328877
Chromosome Location chr2:172915055-172915056
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172907800-172916000 Weak transcription Fetal Kidney kidney
2 chr2:172911000-172930000 Weak transcription Primary T cells from cord blood blood
3 chr2:172911200-172915600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr2:172911200-172947200 Weak transcription HSMM muscle
5 chr2:172911400-172915200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr2:172911400-172916400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr2:172911400-172916600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr2:172911400-172916800 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr2:172912200-172916400 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:172912200-172917000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:172913000-172917000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr2:172913200-172917000 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr2:172913400-172917200 Weak transcription iPS-15b Cell Line embryonic stem cell
14 chr2:172914000-172937000 Weak transcription Pancreas Pancrea
15 chr2:172914400-172916600 Enhancers HepG2 liver
16 chr2:172914400-172916800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr2:172914800-172918000 Enhancers K562 blood
18 chr2:172914800-172918600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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