Variant report

Variant rs560904714
Chromosome Location chr5:17435949-17435950
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17430800-17463800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:17432400-17436000 Weak transcription Placenta Placenta
3 chr5:17434400-17436000 Weak transcription Rectal Smooth Muscle rectum
4 chr5:17434400-17436400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr5:17434600-17436800 Weak transcription Ovary ovary
6 chr5:17435000-17436200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr5:17435200-17436000 Enhancers Primary B cells from cord blood blood
8 chr5:17435400-17436000 Enhancers Monocytes-CD14+_RO01746 blood
9 chr5:17435400-17436400 Enhancers Primary monocytes fromperipheralblood blood
10 chr5:17435400-17436600 Enhancers GM12878-XiMat blood
11 chr5:17435400-17439000 Flanking Active TSS Primary neutrophils fromperipheralblood blood
12 chr5:17435600-17436200 Enhancers Primary hematopoietic stem cells blood
13 chr5:17435800-17436000 Weak transcription Spleen Spleen
14 chr5:17435800-17436200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr5:17435800-17436400 Enhancers Adipose Nuclei Adipose
16 chr5:17435800-17436600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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