Variant report
Variant | rs61835655 |
---|---|
Chromosome Location | chr1:226984108-226984109 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:226966600-226986400 | Weak transcription | Right Atrium | heart |
2 | chr1:226971600-226986800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr1:226976400-226986400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
4 | chr1:226976600-226986400 | Weak transcription | Stomach Smooth Muscle | stomach |
5 | chr1:226977000-226986800 | Weak transcription | Rectal Smooth Muscle | rectum |
6 | chr1:226979400-226984400 | Weak transcription | GM12878-XiMat | blood |
7 | chr1:226982400-226986800 | Weak transcription | HUVEC | blood vessel |
8 | chr1:226983200-226985000 | Weak transcription | Thymus | Thymus |
9 | chr1:226983600-226988600 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |