Variant report
Variant | rs62396773 |
---|---|
Chromosome Location | chr6:15791580-15791581 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:15790600-15792200 | Enhancers | Fetal Brain Female | brain |
2 | chr6:15790600-15793600 | Enhancers | Fetal Intestine Small | intestine |
3 | chr6:15790600-15794600 | Enhancers | Fetal Intestine Large | intestine |
4 | chr6:15790800-15792200 | Enhancers | Fetal Brain Male | brain |
5 | chr6:15790800-15793800 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
6 | chr6:15791000-15792000 | Enhancers | Primary monocytes fromperipheralblood | blood |
7 | chr6:15791000-15792000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
8 | chr6:15791000-15792400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
9 | chr6:15791000-15793800 | Enhancers | Pancreas | Pancrea |
10 | chr6:15791000-15796400 | Enhancers | Skeletal Muscle Female | skeletal muscle |
11 | chr6:15791000-15798000 | Enhancers | Fetal Muscle Leg | muscle |
12 | chr6:15791200-15792000 | Enhancers | Fetal Kidney | kidney |
13 | chr6:15791200-15792000 | Weak transcription | Psoas Muscle | Psoas |
14 | chr6:15791200-15792000 | Enhancers | Stomach Mucosa | stomach |
15 | chr6:15791200-15792800 | Enhancers | K562 | blood |
16 | chr6:15791200-15793200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
17 | chr6:15791200-15793800 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
18 | chr6:15791400-15792000 | Weak transcription | Gastric | stomach |
19 | chr6:15791400-15792200 | Flanking Active TSS | HepG2 | liver |
20 | chr6:15791400-15794400 | Enhancers | HMEC | breast |