Variant report

Variant rs16847213
Chromosome Location chr2:212793611-212793612
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:212788400-212795000 Weak transcription Fetal Heart heart
2 chr2:212791600-212794400 Enhancers Brain Substantia Nigra brain
3 chr2:212791600-212800200 Weak transcription Aorta Aorta
4 chr2:212792200-212796600 Enhancers Cortex derived primary cultured neurospheres brain
5 chr2:212792200-212796800 Enhancers Dnd41 blood
6 chr2:212792400-212794000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr2:212792600-212796400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:212792800-212794400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr2:212792800-212794400 Enhancers Thymus Thymus
10 chr2:212793000-212794400 Enhancers Fetal Thymus thymus
11 chr2:212793200-212793800 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr2:212793400-212794200 Enhancers Brain Anterior Caudate brain
13 chr2:212793600-212793800 Bivalent Enhancer Brain Germinal Matrix brain
14 chr2:212793600-212794000 Enhancers Brain Hippocampus Middle brain
15 chr2:212793600-212794600 Weak transcription Primary T cells from cord blood blood
16 chr2:212793600-212794800 Weak transcription Brain Angular Gyrus brain
17 chr2:212793600-212796200 Weak transcription Brain Cingulate Gyrus brain

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