Variant report

Variant rs10203516
Chromosome Location chr2:190245637-190245638
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190243600-190246400 Enhancers HUES64 Cell Line embryonic stem cell
2 chr2:190243800-190245800 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr2:190243800-190246000 Enhancers HUES6 Cell Line embryonic stem cell
4 chr2:190244600-190246000 Enhancers Muscle Satellite Cultured Cells --
5 chr2:190244800-190245800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr2:190245000-190245800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:190245000-190246000 Enhancers A549 lung
8 chr2:190245000-190257200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:190245600-190245800 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr2:190245600-190245800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr2:190245600-190245800 Enhancers HSMM muscle
12 chr2:190245600-190246000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr2:190245600-190257200 Weak transcription Osteobl bone

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