Variant report

Variant rs34748465
Chromosome Location chr19:53292356-53292357
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:53290600-53292400 Weak transcription Spleen Spleen
2 chr19:53290600-53293200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr19:53290600-53295600 Weak transcription Gastric stomach
4 chr19:53290600-53300000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr19:53290600-53301600 Weak transcription Ovary ovary
6 chr19:53290800-53292600 Enhancers Primary Natural Killer cells fromperipheralblood blood
7 chr19:53290800-53294400 Weak transcription Thymus Thymus
8 chr19:53290800-53302400 Weak transcription Brain Germinal Matrix brain
9 chr19:53291200-53294200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr19:53291200-53297400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr19:53291600-53292400 Weak transcription Brain Substantia Nigra brain
12 chr19:53291600-53292400 Enhancers Dnd41 blood
13 chr19:53291800-53293200 Enhancers HUES6 Cell Line embryonic stem cell
14 chr19:53292200-53292600 Enhancers Placenta Placenta
15 chr19:53292200-53292800 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr19:53292200-53293000 Enhancers HepG2 liver

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