Variant report

Variant rs56069971
Chromosome Location chr5:17406074-17406075
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17399400-17406200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr5:17402800-17406400 Enhancers A549 lung
3 chr5:17403000-17413000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr5:17404400-17407000 Enhancers Stomach Mucosa stomach
5 chr5:17404600-17406200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr5:17404600-17411200 Weak transcription Fetal Brain Male brain
7 chr5:17404800-17406800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr5:17405000-17406200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr5:17405000-17406200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
10 chr5:17405000-17406800 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr5:17405400-17406200 Enhancers NHEK skin
12 chr5:17405600-17407200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr5:17405800-17407200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:17406000-17407200 Enhancers HMEC breast
15 chr5:17406000-17407800 Enhancers Hela-S3 cervix

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