Variant report

Variant rs695056
Chromosome Location chr5:101490273-101490274
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:101488800-101491200 Active TSS ES-I3 Cell Line embryonic stem cell
2 chr5:101489000-101490400 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr5:101489200-101490400 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr5:101489200-101490400 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr5:101489400-101490400 Weak transcription H1 Cell Line embryonic stem cell
6 chr5:101490000-101490400 Active TSS Primary T cells from cord blood blood
7 chr5:101490000-101491200 Active TSS H9 Derived Neuron Cultured Cells ES cell derived
8 chr5:101490200-101491200 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr5:101490200-101491200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
10 chr5:101490200-101491200 Active TSS Primary mononuclear cells fromperipheralblood Blood
11 chr5:101490200-101491200 Active TSS Fetal Intestine Large intestine
12 chr5:101490200-101491200 Active TSS Fetal Intestine Small intestine
13 chr5:101490200-101491200 Active TSS Stomach Smooth Muscle stomach

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