Variant report

Variant rs61996351
Chromosome Location chr22:22380819-22380820
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22376400-22381600 Enhancers Primary B cells from peripheral blood blood
2 chr22:22377400-22385400 Weak transcription Primary hematopoietic stem cells blood
3 chr22:22377600-22385600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr22:22377800-22385200 Weak transcription Right Atrium heart
5 chr22:22379400-22381600 Flanking Active TSS GM12878-XiMat blood
6 chr22:22379800-22381200 Enhancers Primary Natural Killer cells fromperipheralblood blood
7 chr22:22380000-22381000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr22:22380200-22381000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
9 chr22:22380400-22381000 Enhancers Duodenum Mucosa Duodenum
10 chr22:22380400-22381000 Enhancers Rectal Mucosa Donor 29 rectum
11 chr22:22380400-22381200 Enhancers Primary monocytes fromperipheralblood blood
12 chr22:22380400-22381200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr22:22380400-22381400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr22:22380400-22381400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr22:22380600-22381000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr22:22380600-22381000 Enhancers Monocytes-CD14+_RO01746 blood
17 chr22:22380600-22383000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
18 chr22:22380800-22381000 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
19 chr22:22380800-22381000 Flanking Active TSS Primary B cells from cord blood blood

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