Variant report

Variant rs1415600
Chromosome Location chr13:38441493-38441494
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:38436400-38442200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr13:38438000-38442400 Weak transcription Ovary ovary
3 chr13:38438800-38442400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr13:38439000-38441800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr13:38439000-38442800 Weak transcription Colon Smooth Muscle Colon
6 chr13:38440000-38444600 Active TSS iPS-20b Cell Line embryonic stem cell
7 chr13:38440400-38441600 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr13:38440400-38445000 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr13:38440600-38445200 Active TSS Fetal Brain Female brain
10 chr13:38441000-38444600 Active TSS H1 Cell Line embryonic stem cell
11 chr13:38441000-38444600 Active TSS hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr13:38441200-38441600 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr13:38441400-38441600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr13:38441400-38441600 Enhancers NH-A brain
15 chr13:38441400-38441600 Flanking Active TSS Osteobl bone
16 chr13:38441400-38442000 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
17 chr13:38441400-38443000 Active TSS Duodenum Smooth Muscle Duodenum
18 chr13:38441400-38443600 Active TSS Stomach Smooth Muscle stomach
19 chr13:38441400-38444600 Active TSS NHDF-Ad bronchial

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