Variant report

Variant rs559013822
Chromosome Location chr22:30269277-30269278
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:30265800-30270200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr22:30266800-30269400 Enhancers HUES6 Cell Line embryonic stem cell
3 chr22:30266800-30270000 Enhancers Psoas Muscle Psoas
4 chr22:30267600-30269400 Enhancers HUES48 Cell Line embryonic stem cell
5 chr22:30267600-30269400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr22:30267600-30269600 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr22:30267600-30270200 Enhancers Primary monocytes fromperipheralblood blood
8 chr22:30267800-30269400 Enhancers Primary hematopoietic stem cells blood
9 chr22:30267800-30270000 Enhancers Primary B cells from cord blood blood
10 chr22:30268000-30269600 Enhancers Pancreas Pancrea
11 chr22:30268200-30269600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
12 chr22:30268200-30270200 Enhancers Spleen Spleen
13 chr22:30268400-30269400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
14 chr22:30268600-30273800 Weak transcription ES-I3 Cell Line embryonic stem cell
15 chr22:30268800-30269400 Weak transcription Right Atrium heart
16 chr22:30268800-30270000 Enhancers Skeletal Muscle Female skeletal muscle
17 chr22:30268800-30270000 Weak transcription GM12878-XiMat blood
18 chr22:30268800-30277800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr22:30268800-30279000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
20 chr22:30269000-30270200 Enhancers Skeletal Muscle Male skeletal muscle
21 chr22:30269000-30278800 Weak transcription Adipose Nuclei Adipose
22 chr22:30269200-30270200 Enhancers NHEK skin

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