Variant report

Variant rs7285056
Chromosome Location chr22:22378534-22378535
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr22:22376400-22381600 Enhancers Primary B cells from peripheral blood blood
7 chr22:22376800-22378600 Enhancers Fetal Muscle Leg muscle
8 chr22:22376800-22378600 Enhancers HMEC breast
9 chr22:22377000-22378600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr22:22377000-22378800 Flanking Active TSS GM12878-XiMat blood
11 chr22:22377400-22378600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr22:22377400-22379800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr22:22377400-22379800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
14 chr22:22377400-22385400 Weak transcription Primary hematopoietic stem cells blood
15 chr22:22377600-22385600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr22:22377800-22379400 Weak transcription Primary B cells from cord blood blood
17 chr22:22377800-22385200 Weak transcription Right Atrium heart
18 chr22:22378000-22378600 Enhancers HUVEC blood vessel
19 chr22:22378200-22378600 Bivalent Enhancer K562 blood

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