Variant report
Variant | rs6470369 |
---|---|
Chromosome Location | chr8:126647516-126647517 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:126628800-126649400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr8:126638400-126648800 | Weak transcription | Spleen | Spleen |
3 | chr8:126639600-126653600 | Weak transcription | Pancreas | Pancrea |
4 | chr8:126640800-126649200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
5 | chr8:126640800-126649200 | Weak transcription | NHEK | skin |
6 | chr8:126644200-126649200 | Weak transcription | Fetal Lung | lung |
7 | chr8:126645800-126648800 | Weak transcription | Lung | lung |
8 | chr8:126646200-126648800 | Weak transcription | Placenta | Placenta |
9 | chr8:126646200-126649400 | Weak transcription | Adipose Nuclei | Adipose |
10 | chr8:126646400-126650400 | Enhancers | Primary B cells from peripheral blood | blood |
11 | chr8:126646600-126648000 | Enhancers | GM12878-XiMat | blood |
12 | chr8:126647000-126648000 | Weak transcription | Primary B cells from cord blood | blood |
13 | chr8:126647200-126647800 | Bivalent Enhancer | Fetal Muscle Leg | muscle |
14 | chr8:126647200-126649600 | Enhancers | Primary T regulatory cells fromperipheralblood | blood |
15 | chr8:126647400-126647600 | Enhancers | Esophagus | oesophagus |
16 | chr8:126647400-126647600 | Enhancers | Skeletal Muscle Female | skeletal muscle |
17 | chr8:126647400-126648000 | Weak transcription | Small Intestine | intestine |