Variant report

Variant rs3745285
Chromosome Location chr19:41950297-41950298
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41946000-41953000 Weak transcription Right Atrium heart
2 chr19:41946600-41950800 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr19:41946800-41952400 Weak transcription Spleen Spleen
4 chr19:41948000-41957200 Weak transcription Esophagus oesophagus
5 chr19:41948800-41951000 Active TSS Fetal Intestine Large intestine
6 chr19:41948800-41951000 Active TSS Fetal Intestine Small intestine
7 chr19:41949200-41950600 Active TSS Duodenum Mucosa Duodenum
8 chr19:41949200-41952400 Weak transcription Left Ventricle heart
9 chr19:41949400-41953400 Weak transcription Primary monocytes fromperipheralblood blood
10 chr19:41949600-41950400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr19:41949800-41955000 Weak transcription HepG2 liver
12 chr19:41950000-41950400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
13 chr19:41950000-41953000 Weak transcription Lung lung
14 chr19:41950200-41955200 Weak transcription GM12878-XiMat blood

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