Variant report

Variant rs548860220
Chromosome Location chr19:53291600-53291601
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:53290600-53292200 Weak transcription HepG2 liver
2 chr19:53290600-53292400 Weak transcription Spleen Spleen
3 chr19:53290600-53293200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr19:53290600-53295600 Weak transcription Gastric stomach
5 chr19:53290600-53300000 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr19:53290600-53301600 Weak transcription Ovary ovary
7 chr19:53290800-53291600 Enhancers Primary T cells fromperipheralblood blood
8 chr19:53290800-53291800 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr19:53290800-53292600 Enhancers Primary Natural Killer cells fromperipheralblood blood
10 chr19:53290800-53294400 Weak transcription Thymus Thymus
11 chr19:53290800-53302400 Weak transcription Brain Germinal Matrix brain
12 chr19:53291000-53291600 Flanking Active TSS Dnd41 blood
13 chr19:53291200-53291600 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
14 chr19:53291200-53291600 Enhancers Primary T helper naive cells fromperipheralblood blood
15 chr19:53291200-53292200 Weak transcription Placenta Placenta
16 chr19:53291200-53294200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr19:53291200-53297400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
18 chr19:53291600-53292400 Weak transcription Brain Substantia Nigra brain
19 chr19:53291600-53292400 Enhancers Dnd41 blood

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