Variant report

Variant rs6738305
Chromosome Location chr2:51183305-51183306
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51176400-51190600 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr2:51178600-51183600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr2:51179800-51186000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr2:51180400-51184400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:51180400-51184400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr2:51180400-51189400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:51181600-51184000 Weak transcription HMEC breast
8 chr2:51182200-51183400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:51182200-51185200 Weak transcription Fetal Muscle Leg muscle
10 chr2:51182400-51184000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:51183000-51183400 Enhancers Fetal Brain Female brain
12 chr2:51183000-51183400 Active TSS Pancreatic Islets Pancreatic Islet
13 chr2:51183000-51184400 Weak transcription Fetal Kidney kidney
14 chr2:51183000-51185200 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr2:51183200-51184600 Weak transcription Brain Germinal Matrix brain
16 chr2:51183200-51190000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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