Variant report
Variant | rs194785 |
---|---|
Chromosome Location | chr14:69188695-69188696 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:69173600-69194200 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
2 | chr14:69173600-69196400 | Weak transcription | Right Ventricle | heart |
3 | chr14:69176600-69189400 | Weak transcription | Pancreas | Pancrea |
4 | chr14:69181000-69191400 | Weak transcription | Fetal Muscle Trunk | muscle |
5 | chr14:69181000-69195200 | Weak transcription | Spleen | Spleen |
6 | chr14:69182000-69202600 | Weak transcription | Placenta Amnion | Placenta Amnion |
7 | chr14:69182200-69191200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr14:69184800-69188800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
9 | chr14:69187000-69194200 | Weak transcription | HUVEC | blood vessel |
10 | chr14:69187400-69189000 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
11 | chr14:69187400-69200000 | Weak transcription | Primary T killer memory cells from peripheral blood | blood |
12 | chr14:69187600-69189800 | Weak transcription | Small Intestine | intestine |
13 | chr14:69187600-69192400 | Enhancers | Fetal Intestine Small | intestine |
14 | chr14:69187800-69192600 | Weak transcription | K562 | blood |
15 | chr14:69187800-69199400 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
16 | chr14:69188400-69190400 | Enhancers | HepG2 | liver |
17 | chr14:69188400-69193000 | Enhancers | Fetal Intestine Large | intestine |
18 | chr14:69188600-69189200 | Enhancers | Liver | Liver |
19 | chr14:69188600-69190200 | Enhancers | Skeletal Muscle Male | skeletal muscle |
20 | chr14:69188600-69191400 | Enhancers | Duodenum Mucosa | Duodenum |
21 | chr14:69188600-69191800 | Enhancers | Ovary | ovary |
22 | chr14:69188600-69194400 | Weak transcription | Fetal Stomach | stomach |