Variant report

Variant rs2224782
Chromosome Location chr1:172144131-172144132
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172123400-172149200 Weak transcription Brain Anterior Caudate brain
2 chr1:172128400-172149800 Weak transcription Aorta Aorta
3 chr1:172132800-172150000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr1:172138200-172147800 Weak transcription Brain Angular Gyrus brain
5 chr1:172138400-172145000 Weak transcription Placenta Amnion Placenta Amnion
6 chr1:172138400-172149800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:172138600-172147600 Weak transcription Small Intestine intestine
8 chr1:172138600-172147800 Weak transcription Brain Hippocampus Middle brain
9 chr1:172138600-172147800 Weak transcription Brain Inferior Temporal Lobe brain
10 chr1:172139600-172148000 Weak transcription Fetal Stomach stomach
11 chr1:172140200-172146800 Weak transcription Fetal Intestine Small intestine
12 chr1:172142200-172149600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr1:172143600-172145000 Weak transcription Fetal Kidney kidney
14 chr1:172143600-172148000 Weak transcription Colon Smooth Muscle Colon

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