Variant report

Variant rs16852996
Chromosome Location chr2:167990190-167990191
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:167985400-167991000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr2:167985400-167991000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr2:167988600-167990400 Enhancers Skeletal Muscle Male skeletal muscle
4 chr2:167988600-167990400 Enhancers Skeletal Muscle Female skeletal muscle
5 chr2:167988800-167991000 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr2:167989000-167990400 Enhancers Pancreas Pancrea
7 chr2:167989200-167990200 Weak transcription HMEC breast
8 chr2:167989200-167998600 Weak transcription Left Ventricle heart
9 chr2:167989400-167993400 Weak transcription Psoas Muscle Psoas
10 chr2:167989800-167990400 Enhancers Fetal Thymus thymus
11 chr2:167989800-167991000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:167989800-167993400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr2:167989800-167994200 Enhancers Muscle Satellite Cultured Cells --
14 chr2:167990000-167991000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr2:167990000-167991200 Weak transcription HUES64 Cell Line embryonic stem cell
16 chr2:167990000-167991800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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