Variant report

Variant rs4148622
Chromosome Location chr11:17449002-17449003
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17418600-17453600 Weak transcription Fetal Brain Female brain
2 chr11:17428200-17450200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr11:17435200-17460600 Weak transcription Right Atrium heart
4 chr11:17442800-17451200 Weak transcription Brain Inferior Temporal Lobe brain
5 chr11:17443600-17458000 Weak transcription H9 Cell Line embryonic stem cell
6 chr11:17443800-17462600 Weak transcription Brain Substantia Nigra brain
7 chr11:17444000-17450800 Weak transcription Psoas Muscle Psoas
8 chr11:17444200-17452200 Weak transcription Brain Angular Gyrus brain
9 chr11:17446200-17452200 Weak transcription Gastric stomach
10 chr11:17446400-17460600 Weak transcription Fetal Intestine Small intestine
11 chr11:17446600-17452800 Weak transcription Brain Anterior Caudate brain
12 chr11:17447400-17455800 Weak transcription Brain Germinal Matrix brain
13 chr11:17447600-17455400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr11:17447800-17449800 Enhancers Fetal Thymus thymus
15 chr11:17448000-17450600 Strong transcription Pancreatic Islets Pancreatic Islet
16 chr11:17448600-17449200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
17 chr11:17448600-17454200 Enhancers Dnd41 blood

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