Variant report
Variant | rs2919699 |
---|---|
Chromosome Location | chr11:70979929-70979930 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:70977800-70980800 | Weak transcription | Stomach Mucosa | stomach |
2 | chr11:70977800-70981000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr11:70977800-70981200 | Weak transcription | Colonic Mucosa | Colon |
4 | chr11:70978000-70980000 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
5 | chr11:70978000-70980600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr11:70978000-70980600 | Weak transcription | Placenta Amnion | Placenta Amnion |
7 | chr11:70978000-70980800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
8 | chr11:70978000-70981000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr11:70978600-70980600 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr11:70978600-70981600 | Enhancers | Duodenum Mucosa | Duodenum |
11 | chr11:70978800-70980000 | Bivalent Enhancer | Fetal Stomach | stomach |
12 | chr11:70978800-70981600 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
13 | chr11:70979000-70980200 | Enhancers | Pancreas | Pancrea |
14 | chr11:70979200-70980200 | Flanking Active TSS | HepG2 | liver |
15 | chr11:70979200-70981400 | Enhancers | Fetal Intestine Small | intestine |
16 | chr11:70979600-70980400 | Enhancers | Liver | Liver |
17 | chr11:70979600-70980600 | Weak transcription | HSMM | muscle |
18 | chr11:70979600-70980600 | Weak transcription | HSMMtube | muscle |
19 | chr11:70979600-70981600 | Enhancers | A549 | lung |
20 | chr11:70979800-70980000 | Enhancers | Fetal Brain Male | brain |
21 | chr11:70979800-70981600 | Enhancers | Fetal Intestine Large | intestine |