Variant report

Variant rs6000575
Chromosome Location chr22:22376432-22376433
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22372600-22376800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:22373600-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr22:22373800-22378600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr22:22373800-22378600 Enhancers NHEK skin
5 chr22:22374000-22376600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr22:22374200-22376600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr22:22374400-22378600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr22:22374800-22376800 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr22:22375000-22376800 Weak transcription Primary hematopoietic stem cells blood
10 chr22:22375600-22377000 Weak transcription Right Atrium heart
11 chr22:22376000-22377000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr22:22376200-22376600 Weak transcription Pancreas Pancrea
13 chr22:22376200-22377000 Enhancers GM12878-XiMat blood
14 chr22:22376200-22380600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr22:22376400-22376800 Enhancers Fetal Heart heart
16 chr22:22376400-22376800 Weak transcription HMEC breast
17 chr22:22376400-22377200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
18 chr22:22376400-22377800 Enhancers Primary B cells from cord blood blood
19 chr22:22376400-22381600 Enhancers Primary B cells from peripheral blood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links