Variant report

Variant rs191900107
Chromosome Location chr5:115566989-115566990
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:115551800-115576400 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr5:115557400-115580800 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr5:115557400-115583200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
4 chr5:115559200-115578400 Weak transcription Fetal Lung lung
5 chr5:115560400-115570400 Weak transcription Primary B cells from peripheral blood blood
6 chr5:115560400-115572600 Weak transcription Fetal Intestine Small intestine
7 chr5:115560400-115581000 Weak transcription Primary T cells from cord blood blood
8 chr5:115560400-115610600 Weak transcription Left Ventricle heart
9 chr5:115560600-115567600 Weak transcription Primary hematopoietic stem cells blood
10 chr5:115561400-115569400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr5:115561400-115580000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
12 chr5:115561800-115586400 Weak transcription Monocytes-CD14+_RO01746 blood
13 chr5:115562400-115572000 Weak transcription Primary monocytes fromperipheralblood blood
14 chr5:115562400-115589000 Weak transcription Ovary ovary
15 chr5:115563400-115571000 Weak transcription Primary B cells from cord blood blood
16 chr5:115565200-115569200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr5:115565600-115567000 Enhancers Fetal Heart heart
18 chr5:115566600-115567400 Enhancers HepG2 liver

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