Variant report
Variant | rs17023966 |
---|---|
Chromosome Location | chr2:39778628-39778629 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:39762200-39785000 | Weak transcription | HSMMtube | muscle |
2 | chr2:39770800-39789600 | Weak transcription | Left Ventricle | heart |
3 | chr2:39775800-39780400 | Enhancers | HepG2 | liver |
4 | chr2:39776400-39779000 | Enhancers | Fetal Intestine Small | intestine |
5 | chr2:39777000-39778800 | Enhancers | Fetal Heart | heart |
6 | chr2:39777000-39779200 | Enhancers | HUVEC | blood vessel |
7 | chr2:39777400-39778800 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
8 | chr2:39777600-39778800 | Enhancers | Muscle Satellite Cultured Cells | -- |
9 | chr2:39777600-39779200 | Enhancers | Hela-S3 | cervix |
10 | chr2:39778000-39779000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
11 | chr2:39778000-39788000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
12 | chr2:39778400-39791800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |