Variant report

Variant rs10489299
Chromosome Location chr1:172101666-172101667
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172049400-172110800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr1:172062400-172109200 Weak transcription Brain Cingulate Gyrus brain
3 chr1:172069200-172102000 Weak transcription Brain Hippocampus Middle brain
4 chr1:172077200-172110600 Weak transcription Brain Angular Gyrus brain
5 chr1:172085800-172113400 Weak transcription Pancreas Pancrea
6 chr1:172090000-172109600 Weak transcription Brain Germinal Matrix brain
7 chr1:172090400-172108800 Weak transcription Fetal Stomach stomach
8 chr1:172090800-172102200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr1:172092000-172102800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:172094600-172110600 Weak transcription Left Ventricle heart
11 chr1:172095400-172102000 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr1:172096000-172103200 Weak transcription Gastric stomach
13 chr1:172096400-172110600 Weak transcription Brain Substantia Nigra brain
14 chr1:172097600-172102000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
15 chr1:172100200-172108600 Weak transcription Cortex derived primary cultured neurospheres brain
16 chr1:172101200-172107800 Weak transcription Psoas Muscle Psoas
17 chr1:172101600-172103800 Strong transcription Brain Anterior Caudate brain

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