Variant report
Variant | rs9390049 |
---|---|
Chromosome Location | chr6:143376520-143376521 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:143356800-143377000 | Weak transcription | HepG2 | liver |
2 | chr6:143372000-143380400 | Weak transcription | K562 | blood |
3 | chr6:143373600-143380800 | Weak transcription | GM12878-XiMat | blood |
4 | chr6:143374800-143380800 | Weak transcription | Primary T cells from cord blood | blood |
5 | chr6:143375200-143380000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr6:143375200-143381200 | Weak transcription | Aorta | Aorta |
7 | chr6:143375600-143379600 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr6:143375800-143377200 | Enhancers | HUES48 Cell Line | embryonic stem cell |
9 | chr6:143375800-143377200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
10 | chr6:143376000-143380600 | Weak transcription | Adipose Nuclei | Adipose |
11 | chr6:143376200-143380800 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
12 | chr6:143376400-143377200 | Enhancers | H9 Cell Line | embryonic stem cell |
13 | chr6:143376400-143378600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
14 | chr6:143376400-143380200 | Weak transcription | Fetal Intestine Large | intestine |