Variant report

Variant rs34963102
Chromosome Location chr13:95197000-95197001
allele -/A
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:95188600-95200000 Weak transcription Primary T helper cells PMA-I stimulated --
2 chr13:95188800-95200200 Weak transcription Primary T cells from cord blood blood
3 chr13:95195400-95198800 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr13:95195600-95197000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr13:95195600-95200400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr13:95195800-95198600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr13:95195800-95200200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr13:95196400-95197200 Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr13:95196400-95197200 Active TSS H9 Derived Neuron Cultured Cells ES cell derived
10 chr13:95196400-95200800 Weak transcription Pancreas Pancrea
11 chr13:95196600-95197000 Active TSS H9 Cell Line embryonic stem cell
12 chr13:95196600-95200400 Weak transcription Colon Smooth Muscle Colon
13 chr13:95196800-95200600 Weak transcription Fetal Stomach stomach
14 chr13:95197000-95199600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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