Variant report

Variant rs4916255
Chromosome Location chr1:172380875-172380876
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172352400-172386400 Weak transcription Psoas Muscle Psoas
2 chr1:172368400-172390800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr1:172370200-172385600 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr1:172372800-172381600 Weak transcription Brain Inferior Temporal Lobe brain
5 chr1:172373000-172390800 Weak transcription Brain Hippocampus Middle brain
6 chr1:172373000-172390800 Weak transcription Brain Substantia Nigra brain
7 chr1:172373000-172411800 Weak transcription Brain Angular Gyrus brain
8 chr1:172375400-172383600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:172377200-172384400 Weak transcription Placenta Amnion Placenta Amnion
10 chr1:172378400-172385200 Weak transcription Fetal Kidney kidney
11 chr1:172378600-172381200 Weak transcription NHEK skin
12 chr1:172378600-172382800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:172379400-172383600 Weak transcription NHDF-Ad bronchial
14 chr1:172379400-172386600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr1:172379600-172383200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr1:172380800-172381400 Enhancers GM12878-XiMat blood

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