Variant report
| Variant | rs61787829 |
|---|---|
| Chromosome Location | chr1:98390477-98390478 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:98387400-98390600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr1:98387400-98390600 | Weak transcription | HSMM | muscle |
| 3 | chr1:98387600-98390600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 4 | chr1:98387600-98390600 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
| 5 | chr1:98387600-98390600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr1:98387600-98390800 | Weak transcription | Brain Anterior Caudate | brain |
| 7 | chr1:98387600-98390800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
| 8 | chr1:98387800-98390800 | Weak transcription | NHEK | skin |
| 9 | chr1:98387800-98391400 | Weak transcription | HepG2 | liver |
| 10 | chr1:98388200-98390800 | Weak transcription | Small Intestine | intestine |
| 11 | chr1:98388400-98390600 | Weak transcription | Dnd41 | blood |
| 12 | chr1:98388600-98390800 | Weak transcription | Primary T cells from cord blood | blood |
| 13 | chr1:98389200-98393000 | Enhancers | Fetal Intestine Small | intestine |
| 14 | chr1:98389600-98390600 | Weak transcription | Duodenum Mucosa | Duodenum |
| 15 | chr1:98390200-98390600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 16 | chr1:98390200-98391800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 17 | chr1:98390200-98393000 | Enhancers | Fetal Intestine Large | intestine |
