Variant report

Variant rs73383436
Chromosome Location chr22:22464710-22464711
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22455000-22465400 Weak transcription Spleen Spleen
2 chr22:22458000-22465400 Weak transcription Right Atrium heart
3 chr22:22463200-22465000 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr22:22463800-22464800 Flanking Active TSS K562 blood
5 chr22:22463800-22465000 Enhancers Primary B cells from cord blood blood
6 chr22:22463800-22468200 Enhancers Primary B cells from peripheral blood blood
7 chr22:22464000-22465000 Enhancers NHEK skin
8 chr22:22464000-22465200 Enhancers GM12878-XiMat blood
9 chr22:22464000-22466600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr22:22464000-22466800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr22:22464200-22465600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr22:22464200-22466600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr22:22464400-22466200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr22:22464400-22467000 Enhancers HMEC breast
15 chr22:22464600-22466200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
16 chr22:22464600-22466800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr22:22464600-22467600 Enhancers Monocytes-CD14+_RO01746 blood

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