Variant report

Variant rs11834856
Chromosome Location chr12:57373480-57373481
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:57361800-57389000 Weak transcription Aorta Aorta
2 chr12:57370800-57379800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr12:57370800-57381200 Weak transcription Brain Anterior Caudate brain
4 chr12:57371600-57381000 Weak transcription Brain Inferior Temporal Lobe brain
5 chr12:57372000-57384800 Weak transcription Gastric stomach
6 chr12:57372200-57384800 Weak transcription Primary T cells from cord blood blood
7 chr12:57372400-57374400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr12:57372400-57375000 Enhancers Esophagus oesophagus
9 chr12:57372600-57375000 Weak transcription Fetal Muscle Leg muscle
10 chr12:57372600-57381000 Weak transcription Spleen Spleen
11 chr12:57372800-57381000 Weak transcription Stomach Smooth Muscle stomach
12 chr12:57373200-57373800 Enhancers Placenta Amnion Placenta Amnion
13 chr12:57373200-57374200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr12:57373200-57374600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr12:57373200-57388600 Weak transcription Fetal Brain Female brain
16 chr12:57373200-57388800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr12:57373400-57373800 Enhancers Lung lung
18 chr12:57373400-57373800 Enhancers K562 blood
19 chr12:57373400-57374400 Enhancers HMEC breast

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