Variant report

Variant rs881829
Chromosome Location chr6:162960201-162960202
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162941200-162989400 Weak transcription Aorta Aorta
2 chr6:162955000-162973200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:162959000-162961000 Enhancers Fetal Heart heart
4 chr6:162959200-162960400 Enhancers Fetal Brain Male brain
5 chr6:162959200-162960800 Enhancers Fetal Muscle Leg muscle
6 chr6:162959600-162960600 Enhancers Brain Anterior Caudate brain
7 chr6:162959600-162960800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr6:162959600-162960800 Enhancers Fetal Brain Female brain
9 chr6:162959600-162960800 Enhancers Pancreatic Islets Pancreatic Islet
10 chr6:162959800-162960600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr6:162959800-162960600 Enhancers Fetal Stomach stomach
12 chr6:162959800-162960800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:162959800-162960800 Enhancers Cortex derived primary cultured neurospheres brain
14 chr6:162959800-162962000 Weak transcription Left Ventricle heart
15 chr6:162960200-162960400 Enhancers Brain Germinal Matrix brain
16 chr6:162960200-162978200 Weak transcription Psoas Muscle Psoas

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