Variant report
Variant | rs2110078 |
---|---|
Chromosome Location | chr12:9015359-9015360 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:8982200-9022000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr12:8983400-9017600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr12:8987600-9040000 | Weak transcription | H1 Cell Line | embryonic stem cell |
4 | chr12:8994800-9016600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
5 | chr12:8996000-9040000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
6 | chr12:8999000-9016400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
7 | chr12:9005200-9017800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
8 | chr12:9007000-9029600 | Weak transcription | H9 Cell Line | embryonic stem cell |
9 | chr12:9007200-9027600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr12:9011800-9021600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
11 | chr12:9011800-9029800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
12 | chr12:9012600-9020400 | Weak transcription | Esophagus | oesophagus |
13 | chr12:9013600-9019200 | Weak transcription | K562 | blood |
14 | chr12:9013600-9029400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
15 | chr12:9013800-9033800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |