Variant report

Variant rs73984068
Chromosome Location chr2:210385778-210385779
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210364600-210387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr2:210364600-210392200 Weak transcription Pancreas Pancrea
3 chr2:210366600-210387800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:210371400-210391000 Weak transcription Aorta Aorta
5 chr2:210378800-210385800 Weak transcription Fetal Brain Male brain
6 chr2:210378800-210390200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:210382200-210391600 Enhancers Cortex derived primary cultured neurospheres brain
8 chr2:210383000-210391000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr2:210383200-210386200 Enhancers Brain Germinal Matrix brain
10 chr2:210384000-210386000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
11 chr2:210384000-210386000 Enhancers Fetal Brain Female brain
12 chr2:210384000-210386600 Enhancers Pancreatic Islets Pancreatic Islet
13 chr2:210384000-210388600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr2:210384800-210385800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
15 chr2:210384800-210385800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr2:210385200-210387000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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