Variant report
Variant | rs11643101 |
---|---|
Chromosome Location | chr16:71459439-71459440 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:71446800-71459600 | Weak transcription | Spleen | Spleen |
2 | chr16:71457000-71461000 | Weak transcription | Right Atrium | heart |
3 | chr16:71458400-71459600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr16:71458800-71459600 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr16:71459000-71459600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
6 | chr16:71459200-71459600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
7 | chr16:71459200-71459600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
8 | chr16:71459200-71459800 | Bivalent/Poised TSS | HUES6 Cell Line | embryonic stem cell |
9 | chr16:71459200-71460000 | Bivalent/Poised TSS | ES-I3 Cell Line | embryonic stem cell |
10 | chr16:71459200-71461200 | Bivalent/Poised TSS | iPS-20b Cell Line | embryonic stem cell |
11 | chr16:71459400-71459600 | Bivalent/Poised TSS | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
12 | chr16:71459400-71459600 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin02 | Skin |
13 | chr16:71459400-71459600 | Bivalent Enhancer | Foreskin Keratinocyte Primary Cells skin02 | Skin |
14 | chr16:71459400-71459600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
15 | chr16:71459400-71459800 | Flanking Active TSS | HepG2 | liver |
16 | chr16:71459400-71460000 | Bivalent/Poised TSS | iPS-18 Cell Line | embryonic stem cell |
17 | chr16:71459400-71460800 | Active TSS | H1 Cell Line | embryonic stem cell |
18 | chr16:71459400-71460800 | Active TSS | H9 Cell Line | embryonic stem cell |
19 | chr16:71459400-71460800 | Bivalent/Poised TSS | HUES64 Cell Line | embryonic stem cell |
20 | chr16:71459400-71461000 | Active TSS | iPS-15b Cell Line | embryonic stem cell |