Variant report
Variant | rs41298121 |
---|---|
Chromosome Location | chr11:74916847-74916848 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:74907800-74918000 | Weak transcription | Right Atrium | heart |
2 | chr11:74911400-74919800 | Weak transcription | Spleen | Spleen |
3 | chr11:74913800-74918000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
4 | chr11:74914200-74917200 | Genic enhancers | Fetal Intestine Small | intestine |
5 | chr11:74914400-74917200 | Enhancers | Fetal Intestine Large | intestine |
6 | chr11:74915800-74919600 | Weak transcription | Lung | lung |
7 | chr11:74916000-74918600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
8 | chr11:74916000-74919600 | Weak transcription | Pancreas | Pancrea |
9 | chr11:74916000-74920800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr11:74916400-74918600 | Weak transcription | Fetal Muscle Leg | muscle |
11 | chr11:74916400-74919200 | Weak transcription | K562 | blood |
12 | chr11:74916800-74919600 | Weak transcription | Liver | Liver |