Variant report

Variant rs1723251
Chromosome Location chr7:14787171-14787172
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:14784400-14789400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:14785800-14792200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr7:14786000-14787200 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr7:14786600-14788200 Enhancers Brain Hippocampus Middle brain
5 chr7:14786800-14787600 Enhancers HUVEC blood vessel
6 chr7:14786800-14788200 Enhancers Fetal Lung lung
7 chr7:14786800-14788400 Enhancers Brain Substantia Nigra brain
8 chr7:14787000-14787200 Enhancers Brain Inferior Temporal Lobe brain
9 chr7:14787000-14787400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr7:14787000-14787400 Enhancers Brain Cingulate Gyrus brain
11 chr7:14787000-14787400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
12 chr7:14787000-14787600 Enhancers Fetal Brain Male brain
13 chr7:14787000-14788200 Enhancers NH-A brain
14 chr7:14787000-14788400 Enhancers Brain Angular Gyrus brain
15 chr7:14787000-14789000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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