Variant report
Variant | rs9496519 |
---|---|
Chromosome Location | chr6:143413584-143413585 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:143382600-143426800 | Weak transcription | Ovary | ovary |
2 | chr6:143386400-143431800 | Weak transcription | NHEK | skin |
3 | chr6:143389600-143437000 | Weak transcription | HSMM | muscle |
4 | chr6:143389800-143418800 | Weak transcription | Osteobl | bone |
5 | chr6:143395800-143432200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr6:143397400-143431600 | Weak transcription | HMEC | breast |
7 | chr6:143402200-143418400 | Weak transcription | K562 | blood |
8 | chr6:143403200-143417400 | Weak transcription | Stomach Mucosa | stomach |
9 | chr6:143404000-143417800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr6:143404000-143422600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
11 | chr6:143408200-143418600 | Weak transcription | Left Ventricle | heart |
12 | chr6:143408600-143445400 | Weak transcription | Aorta | Aorta |
13 | chr6:143408600-143452600 | Weak transcription | Right Ventricle | heart |
14 | chr6:143408800-143417200 | Weak transcription | Fetal Intestine Small | intestine |
15 | chr6:143409800-143413600 | Weak transcription | HepG2 | liver |
16 | chr6:143412200-143416000 | Weak transcription | Liver | Liver |
17 | chr6:143412200-143417600 | Weak transcription | Primary T cells from cord blood | blood |
18 | chr6:143412400-143413600 | Weak transcription | Brain Substantia Nigra | brain |
19 | chr6:143412400-143417600 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
20 | chr6:143412400-143420400 | Weak transcription | Brain Inferior Temporal Lobe | brain |