Variant report

Variant rs443725
Chromosome Location chr5:178797837-178797838
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178795000-178798600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:178796000-178798000 Weak transcription Fetal Brain Female brain
3 chr5:178796200-178798000 Weak transcription Fetal Brain Male brain
4 chr5:178797000-178801200 Weak transcription Spleen Spleen
5 chr5:178797200-178799400 Enhancers Brain Hippocampus Middle brain
6 chr5:178797200-178800800 Enhancers Cortex derived primary cultured neurospheres brain
7 chr5:178797400-178799200 Enhancers Brain Cingulate Gyrus brain
8 chr5:178797600-178798800 Enhancers Brain Inferior Temporal Lobe brain
9 chr5:178797600-178798800 Enhancers Brain Substantia Nigra brain
10 chr5:178797600-178799000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
11 chr5:178797600-178799200 Enhancers Brain Angular Gyrus brain
12 chr5:178797800-178798600 Enhancers Esophagus oesophagus
13 chr5:178797800-178799000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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