Variant report

Variant rs13426488
Chromosome Location chr2:58929702-58929703
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:58928800-58929800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr2:58928800-58930200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:58928800-58931400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr2:58929000-58929800 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr2:58929000-58930200 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr2:58929000-58930200 Enhancers HMEC breast
7 chr2:58929000-58930200 Enhancers HUVEC blood vessel
8 chr2:58929000-58930600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr2:58929200-58929800 Enhancers Primary monocytes fromperipheralblood blood
10 chr2:58929200-58930000 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr2:58929200-58930000 Enhancers HUES6 Cell Line embryonic stem cell
12 chr2:58929200-58930200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr2:58929200-58930200 Enhancers HepG2 liver
14 chr2:58929200-58930400 Enhancers NH-A brain
15 chr2:58929200-58931000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr2:58929400-58935600 Weak transcription K562 blood
17 chr2:58929600-58930200 Enhancers HUES48 Cell Line embryonic stem cell

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