Variant report

Variant rs78558703
Chromosome Location chr12:31399992-31399993
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31395200-31405200 Weak transcription Right Atrium heart
2 chr12:31398600-31400400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr12:31398600-31400400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:31398800-31400000 Enhancers Fetal Heart heart
5 chr12:31399200-31400000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr12:31399200-31405000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:31399400-31400000 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr12:31399400-31400200 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr12:31399400-31400200 Enhancers HSMMtube muscle
10 chr12:31399800-31400000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr12:31399800-31400200 Enhancers HepG2 liver
12 chr12:31399800-31400200 Enhancers NHEK skin
13 chr12:31399800-31400400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr12:31399800-31400400 Enhancers HMEC breast
15 chr12:31399800-31405200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr12:31399800-31412600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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