Variant report

Variant rs288055
Chromosome Location chr2:210387732-210387733
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210364600-210392200 Weak transcription Pancreas Pancrea
2 chr2:210366600-210387800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:210371400-210391000 Weak transcription Aorta Aorta
4 chr2:210378800-210390200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:210382200-210391600 Enhancers Cortex derived primary cultured neurospheres brain
6 chr2:210383000-210391000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:210384000-210388600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr2:210386200-210388200 Weak transcription HUVEC blood vessel
9 chr2:210386600-210388200 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr2:210386800-210389600 Enhancers Fetal Brain Male brain
11 chr2:210387000-210389000 Enhancers Fetal Brain Female brain
12 chr2:210387000-210391600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr2:210387200-210389800 Enhancers Brain Germinal Matrix brain
14 chr2:210387600-210388200 Enhancers NH-A brain
15 chr2:210387600-210388800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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