Variant report

Variant rs148891269
Chromosome Location chr12:41224078-41224079
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:41221800-41224600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr12:41222600-41224200 Enhancers Pancreatic Islets Pancreatic Islet
3 chr12:41222800-41228000 Weak transcription Fetal Brain Male brain
4 chr12:41223200-41224200 Enhancers NHEK skin
5 chr12:41223400-41224200 Flanking Active TSS A549 lung
6 chr12:41223800-41224200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr12:41224000-41224200 Enhancers Brain Inferior Temporal Lobe brain
8 chr12:41224000-41225200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr12:41224000-41225200 Weak transcription HMEC breast
10 chr12:41224000-41225600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr12:41224000-41226600 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr12:41224000-41228200 Weak transcription Fetal Brain Female brain

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