Variant report

Variant rs12319614
Chromosome Location chr12:31225289-31225290
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31189800-31225400 Weak transcription Fetal Stomach stomach
2 chr12:31219600-31225600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr12:31221000-31225600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:31221200-31225400 Weak transcription HMEC breast
5 chr12:31221200-31225600 Weak transcription NHEK skin
6 chr12:31221400-31225600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr12:31221600-31225600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:31225200-31225400 Enhancers H1 Cell Line embryonic stem cell
9 chr12:31225200-31225400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr12:31225200-31225400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr12:31225200-31225400 Active TSS Fetal Thymus thymus
12 chr12:31225200-31225400 Active TSS Hela-S3 cervix
13 chr12:31225200-31225600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr12:31225200-31225600 Enhancers HepG2 liver
15 chr12:31225200-31225600 Enhancers K562 blood
16 chr12:31225200-31225800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr12:31225200-31226200 Flanking Active TSS Dnd41 blood
18 chr12:31225200-31228000 Active TSS ES-I3 Cell Line embryonic stem cell
19 chr12:31225200-31228400 Active TSS HUES6 Cell Line embryonic stem cell
20 chr12:31225200-31228600 Active TSS iPS-20b Cell Line embryonic stem cell

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