Variant report
Variant | rs10021697 |
---|---|
Chromosome Location | chr4:110935023-110935024 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:110910400-110935200 | Weak transcription | Pancreas | Pancrea |
2 | chr4:110919000-110935200 | Weak transcription | Left Ventricle | heart |
3 | chr4:110920800-110935800 | Strong transcription | Skeletal Muscle Female | skeletal muscle |
4 | chr4:110930000-110937200 | Weak transcription | Fetal Intestine Small | intestine |
5 | chr4:110930400-110941600 | Weak transcription | Fetal Heart | heart |
6 | chr4:110930800-110941600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr4:110931000-110937000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
8 | chr4:110931000-110937600 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
9 | chr4:110931000-110941600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
10 | chr4:110931200-110935200 | Weak transcription | Fetal Kidney | kidney |
11 | chr4:110934600-110935400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
12 | chr4:110935000-110935600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |