Variant report
Variant | rs6758258 |
---|---|
Chromosome Location | chr2:55310942-55310943 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:55299200-55318000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr2:55308800-55312000 | Enhancers | Primary monocytes fromperipheralblood | blood |
3 | chr2:55309200-55312000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
4 | chr2:55309200-55315200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
5 | chr2:55310000-55311200 | Enhancers | Hela-S3 | cervix |
6 | chr2:55310200-55311000 | Enhancers | Primary B cells from cord blood | blood |
7 | chr2:55310200-55313400 | Enhancers | Fetal Lung | lung |
8 | chr2:55310400-55311000 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
9 | chr2:55310600-55311000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
10 | chr2:55310600-55311000 | Flanking Active TSS | HUVEC | blood vessel |
11 | chr2:55310800-55312200 | Enhancers | Adipose Nuclei | Adipose |