Variant report
| Variant | rs6696916 |
|---|---|
| Chromosome Location | chr1:184192465-184192466 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:184180200-184194400 | Weak transcription | Fetal Brain Male | brain |
| 2 | chr1:184182400-184193400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr1:184182400-184195400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr1:184191800-184192800 | Active TSS | Brain Dorsolateral Prefrontal Cortex | brain |
| 5 | chr1:184191800-184192800 | Active TSS | A549 | lung |
| 6 | chr1:184191800-184194600 | Weak transcription | Fetal Brain Female | brain |
| 7 | chr1:184192000-184192800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 8 | chr1:184192200-184192600 | Bivalent Enhancer | HUES48 Cell Line | embryonic stem cell |
| 9 | chr1:184192200-184192800 | Bivalent/Poised TSS | HUES6 Cell Line | embryonic stem cell |
| 10 | chr1:184192200-184194600 | Weak transcription | Brain Substantia Nigra | brain |
| 11 | chr1:184192400-184192600 | Bivalent Enhancer | H1 Cell Line | embryonic stem cell |
| 12 | chr1:184192400-184192600 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 13 | chr1:184192400-184192600 | Flanking Bivalent TSS/Enh | iPS-15b Cell Line | embryonic stem cell |
| 14 | chr1:184192400-184192600 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 15 | chr1:184192400-184192600 | Bivalent/Poised TSS | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 16 | chr1:184192400-184192800 | Bivalent Enhancer | ES-I3 Cell Line | embryonic stem cell |
