Variant report

Variant rs13185339
Chromosome Location chr5:58264673-58264674
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:58255200-58270200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:58259600-58266800 Weak transcription HSMM muscle
3 chr5:58260200-58270200 Weak transcription HSMMtube muscle
4 chr5:58262000-58268800 Weak transcription Primary T cells fromperipheralblood blood
5 chr5:58262400-58269000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr5:58262400-58273400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr5:58262800-58268200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr5:58263200-58270000 Weak transcription Small Intestine intestine
9 chr5:58263200-58271400 Weak transcription Primary T helper naive cells from peripheral blood blood
10 chr5:58263800-58270000 Weak transcription Left Ventricle heart
11 chr5:58263800-58270200 Weak transcription Brain Angular Gyrus brain
12 chr5:58264000-58270200 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr5:58264000-58270200 Weak transcription Gastric stomach
14 chr5:58264200-58270000 Weak transcription Fetal Brain Female brain
15 chr5:58264400-58266800 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr5:58264400-58270000 Genic enhancers A549 lung
17 chr5:58264600-58270200 Weak transcription Spleen Spleen

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