Variant report
Variant | rs4902623 |
---|---|
Chromosome Location | chr14:69110926-69110927 |
allele | A/C/G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:69105000-69121600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr14:69105600-69113000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr14:69105800-69113200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
4 | chr14:69106000-69117000 | Weak transcription | Fetal Intestine Large | intestine |
5 | chr14:69106200-69112800 | Weak transcription | H9 Cell Line | embryonic stem cell |
6 | chr14:69106200-69115600 | Weak transcription | Esophagus | oesophagus |
7 | chr14:69106400-69118200 | Weak transcription | Placenta Amnion | Placenta Amnion |
8 | chr14:69106400-69118400 | Weak transcription | Spleen | Spleen |
9 | chr14:69106600-69111000 | Weak transcription | Fetal Heart | heart |
10 | chr14:69106600-69111800 | Weak transcription | Rectal Smooth Muscle | rectum |
11 | chr14:69106800-69116000 | Weak transcription | Ovary | ovary |
12 | chr14:69108800-69119000 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
13 | chr14:69109400-69122400 | Weak transcription | Primary B cells from cord blood | blood |
14 | chr14:69109800-69111400 | Enhancers | Fetal Stomach | stomach |
15 | chr14:69110200-69111000 | Enhancers | Adipose Nuclei | Adipose |
16 | chr14:69110400-69111200 | Enhancers | Fetal Muscle Leg | muscle |
17 | chr14:69110600-69111200 | Enhancers | Right Ventricle | heart |
18 | chr14:69110800-69111000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
19 | chr14:69110800-69111200 | Enhancers | Fetal Muscle Trunk | muscle |
20 | chr14:69110800-69111400 | Enhancers | Stomach Smooth Muscle | stomach |