Variant report

Variant rs10407348
Chromosome Location chr19:41953430-41953431
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41948000-41957200 Weak transcription Esophagus oesophagus
2 chr19:41949800-41955000 Weak transcription HepG2 liver
3 chr19:41950200-41955200 Weak transcription GM12878-XiMat blood
4 chr19:41952400-41953600 Active TSS Left Ventricle heart
5 chr19:41952400-41954000 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
6 chr19:41952600-41954000 Weak transcription Fetal Intestine Large intestine
7 chr19:41953000-41954200 Active TSS Right Atrium heart
8 chr19:41953200-41954000 Bivalent/Poised TSS Adipose Nuclei Adipose
9 chr19:41953200-41954200 Active TSS Right Ventricle heart
10 chr19:41953200-41955200 Bivalent Enhancer Primary T cells fromperipheralblood blood
11 chr19:41953200-41955600 Weak transcription Spleen Spleen
12 chr19:41953400-41954000 Enhancers Primary monocytes fromperipheralblood blood
13 chr19:41953400-41954200 Weak transcription Lung lung
14 chr19:41953400-41954800 Weak transcription Fetal Intestine Small intestine
15 chr19:41953400-41958600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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