Variant report

Variant rs12159720
Chromosome Location chr22:22377206-22377207
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22373600-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr22:22373800-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr22:22373800-22378600 Enhancers NHEK skin
4 chr22:22374400-22378600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr22:22376200-22380600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr22:22376400-22377800 Enhancers Primary B cells from cord blood blood
7 chr22:22376400-22381600 Enhancers Primary B cells from peripheral blood blood
8 chr22:22376600-22377600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr22:22376800-22377400 Enhancers Primary hematopoietic stem cells blood
10 chr22:22376800-22377400 Enhancers Primary Natural Killer cells fromperipheralblood blood
11 chr22:22376800-22378400 Enhancers Fetal Muscle Trunk muscle
12 chr22:22376800-22378600 Enhancers Fetal Muscle Leg muscle
13 chr22:22376800-22378600 Enhancers HMEC breast
14 chr22:22377000-22377400 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr22:22377000-22378200 Enhancers K562 blood
16 chr22:22377000-22378600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr22:22377000-22378800 Flanking Active TSS GM12878-XiMat blood
18 chr22:22377200-22377800 Strong transcription Right Atrium heart

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