Variant report
Variant | rs35199438 |
---|---|
Chromosome Location | chr11:16630779-16630780 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16629800-16634200 | Weak transcription | Pancreas | Pancrea |
2 | chr11:16630000-16633200 | Weak transcription | Right Atrium | heart |
3 | chr11:16630000-16633600 | Weak transcription | Left Ventricle | heart |
4 | chr11:16630000-16633600 | Weak transcription | Right Ventricle | heart |
5 | chr11:16630000-16634200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr11:16630000-16634200 | Weak transcription | Psoas Muscle | Psoas |
7 | chr11:16630000-16634400 | Weak transcription | K562 | blood |
8 | chr11:16630200-16630800 | Enhancers | Fetal Heart | heart |
9 | chr11:16630200-16631200 | Enhancers | Cortex derived primary cultured neurospheres | brain |
10 | chr11:16630200-16631600 | Enhancers | Brain Germinal Matrix | brain |
11 | chr11:16630600-16631000 | Flanking Active TSS | Ganglion Eminence derived primary cultured neurospheres | brain |
12 | chr11:16630600-16633200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
13 | chr11:16630600-16633800 | Bivalent/Poised TSS | iPS-15b Cell Line | embryonic stem cell |