Variant report

Variant rs73417667
Chromosome Location chr7:104487770-104487771
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:104476400-104503000 Weak transcription Duodenum Mucosa Duodenum
2 chr7:104479600-104488800 Weak transcription Colon Smooth Muscle Colon
3 chr7:104481600-104514400 Weak transcription Fetal Kidney kidney
4 chr7:104483600-104493000 Weak transcription Pancreas Pancrea
5 chr7:104486000-104489400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr7:104486200-104487800 Enhancers Brain Substantia Nigra brain
7 chr7:104486200-104489200 Enhancers Brain Cingulate Gyrus brain
8 chr7:104486200-104492800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr7:104486600-104492600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr7:104486800-104488600 Weak transcription Brain Anterior Caudate brain
11 chr7:104486800-104491000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr7:104487000-104487800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr7:104487200-104488200 Weak transcription Fetal Intestine Large intestine
14 chr7:104487400-104488600 Weak transcription Brain Hippocampus Middle brain
15 chr7:104487400-104490000 Strong transcription Fetal Intestine Small intestine
16 chr7:104487600-104487800 Enhancers Brain Inferior Temporal Lobe brain

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