Variant report

Variant rs391406
Chromosome Location chr22:22374383-22374384
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22365800-22375600 Weak transcription GM12878-XiMat blood
2 chr22:22365800-22376400 Weak transcription Primary B cells from peripheral blood blood
3 chr22:22370600-22374400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr22:22372400-22374800 Bivalent Enhancer K562 blood
5 chr22:22372600-22376800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr22:22372800-22374400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr22:22373400-22374400 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr22:22373600-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr22:22373800-22374800 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr22:22373800-22376000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr22:22373800-22376400 Enhancers HMEC breast
12 chr22:22373800-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr22:22373800-22378600 Enhancers NHEK skin
14 chr22:22374000-22376600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr22:22374200-22376600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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