Variant report

Variant rs168057
Chromosome Location chr13:110496726-110496727
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110489600-110497200 Weak transcription Stomach Mucosa stomach
2 chr13:110493000-110497800 Enhancers Muscle Satellite Cultured Cells --
3 chr13:110493200-110498600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr13:110493200-110499200 Weak transcription Right Atrium heart
5 chr13:110493800-110496800 Weak transcription HMEC breast
6 chr13:110493800-110497000 Weak transcription NH-A brain
7 chr13:110494000-110497000 Weak transcription HSMMtube muscle
8 chr13:110495800-110497200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr13:110496000-110497600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr13:110496200-110497600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr13:110496200-110497600 Enhancers Rectal Smooth Muscle rectum
12 chr13:110496600-110496800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr13:110496600-110497000 Active TSS Colon Smooth Muscle Colon
14 chr13:110496600-110497000 Enhancers Skeletal Muscle Male skeletal muscle
15 chr13:110496600-110497200 Enhancers Osteobl bone
16 chr13:110496600-110497400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr13:110496600-110497400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
18 chr13:110496600-110497400 Enhancers Fetal Heart heart
19 chr13:110496600-110497400 Active TSS Stomach Smooth Muscle stomach
20 chr13:110496600-110497600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
21 chr13:110496600-110497600 Enhancers Cortex derived primary cultured neurospheres brain
22 chr13:110496600-110497600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
23 chr13:110496600-110497600 Enhancers HSMM muscle

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