Variant report

Variant rs1716609
Chromosome Location chr12:44770767-44770768
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44699000-44782000 Weak transcription Aorta Aorta
2 chr12:44754000-44775600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr12:44762000-44777400 Weak transcription Fetal Intestine Small intestine
4 chr12:44762000-44791200 Weak transcription Fetal Intestine Large intestine
5 chr12:44766600-44771400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr12:44767200-44770800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr12:44767400-44773000 Weak transcription HMEC breast
8 chr12:44768200-44773400 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr12:44769000-44772400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr12:44769800-44772000 Weak transcription Brain Hippocampus Middle brain
11 chr12:44769800-44773800 Weak transcription Psoas Muscle Psoas
12 chr12:44770000-44784400 Weak transcription Pancreas Pancrea
13 chr12:44770000-44785200 Weak transcription Adipose Nuclei Adipose
14 chr12:44770200-44774200 Weak transcription HSMMtube muscle
15 chr12:44770400-44771200 Strong transcription Left Ventricle heart
16 chr12:44770600-44770800 Enhancers Placenta Amnion Placenta Amnion
17 chr12:44770600-44772800 Weak transcription Primary T helper cells PMA-I stimulated --

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