Variant report
Variant | rs150858007 |
---|---|
Chromosome Location | chr2:86620007-86620008 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:86615000-86620200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr2:86615800-86620200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
3 | chr2:86619600-86620800 | Enhancers | Left Ventricle | heart |
4 | chr2:86619600-86621200 | Enhancers | Fetal Muscle Leg | muscle |
5 | chr2:86619600-86621600 | Enhancers | Fetal Intestine Large | intestine |
6 | chr2:86619600-86622000 | Enhancers | Fetal Intestine Small | intestine |
7 | chr2:86619800-86620400 | Enhancers | Fetal Heart | heart |
8 | chr2:86619800-86621800 | Enhancers | HSMMtube | muscle |
9 | chr2:86619800-86622800 | Enhancers | Psoas Muscle | Psoas |
10 | chr2:86620000-86621000 | Enhancers | Duodenum Mucosa | Duodenum |
11 | chr2:86620000-86621000 | Enhancers | Rectal Mucosa Donor 31 | rectum |
12 | chr2:86620000-86621600 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
13 | chr2:86620000-86621600 | Enhancers | Primary T helper naive cells from peripheral blood | blood |
14 | chr2:86620000-86621600 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
15 | chr2:86620000-86621600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
16 | chr2:86620000-86621600 | Enhancers | Colonic Mucosa | Colon |
17 | chr2:86620000-86621600 | Enhancers | HSMM | muscle |