Variant report

Variant rs28516927
Chromosome Location chr13:110494383-110494384
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110488400-110496200 Weak transcription Aorta Aorta
2 chr13:110489600-110497200 Weak transcription Stomach Mucosa stomach
3 chr13:110491000-110494800 Enhancers HSMM muscle
4 chr13:110492800-110496600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr13:110493000-110495200 Weak transcription Right Ventricle heart
6 chr13:110493000-110495600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr13:110493000-110496600 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr13:110493000-110497800 Enhancers Muscle Satellite Cultured Cells --
9 chr13:110493200-110498600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr13:110493200-110499200 Weak transcription Right Atrium heart
11 chr13:110493600-110496200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr13:110493600-110496600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr13:110493600-110496600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr13:110493600-110496600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr13:110493600-110496600 Weak transcription Osteobl bone
16 chr13:110493800-110495000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr13:110493800-110496800 Weak transcription HMEC breast
18 chr13:110493800-110497000 Weak transcription NH-A brain
19 chr13:110494000-110496000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
20 chr13:110494000-110497000 Weak transcription HSMMtube muscle
21 chr13:110494200-110494600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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