Variant report
Variant | rs11023919 |
---|---|
Chromosome Location | chr11:16357754-16357755 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16319400-16377600 | Weak transcription | Psoas Muscle | Psoas |
2 | chr11:16345800-16367000 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
3 | chr11:16348400-16362600 | Weak transcription | Left Ventricle | heart |
4 | chr11:16348800-16368600 | Weak transcription | Brain Germinal Matrix | brain |
5 | chr11:16349600-16357800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
6 | chr11:16351000-16360000 | Weak transcription | Fetal Heart | heart |
7 | chr11:16353000-16361400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr11:16354800-16360400 | Enhancers | Pancreatic Islets | Pancreatic Islet |
9 | chr11:16356400-16358200 | Enhancers | Fetal Intestine Small | intestine |
10 | chr11:16356600-16358200 | Enhancers | Rectal Mucosa Donor 31 | rectum |
11 | chr11:16356800-16357800 | Enhancers | Rectal Mucosa Donor 29 | rectum |
12 | chr11:16356800-16358200 | Enhancers | HepG2 | liver |
13 | chr11:16356800-16360800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
14 | chr11:16357000-16358400 | Enhancers | Fetal Kidney | kidney |
15 | chr11:16357200-16357800 | Enhancers | K562 | blood |
16 | chr11:16357400-16360200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
17 | chr11:16357400-16360200 | Enhancers | Fetal Intestine Large | intestine |
18 | chr11:16357600-16358000 | Genic enhancers | Cortex derived primary cultured neurospheres | brain |
19 | chr11:16357600-16358200 | Flanking Active TSS | Duodenum Mucosa | Duodenum |