Variant report

Variant rs547319500
Chromosome Location chr7:4296052-4296053
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4285600-4301200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr7:4287600-4304200 Weak transcription Gastric stomach
3 chr7:4288000-4300800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr7:4288600-4297800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr7:4289200-4304000 Weak transcription Pancreas Pancrea
6 chr7:4291400-4304200 Weak transcription Aorta Aorta
7 chr7:4294600-4298200 Enhancers Fetal Stomach stomach
8 chr7:4294800-4311800 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr7:4295600-4297600 Enhancers Fetal Brain Male brain
10 chr7:4295800-4296200 Enhancers Colon Smooth Muscle Colon
11 chr7:4295800-4297000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr7:4295800-4297400 Enhancers Fetal Lung lung
13 chr7:4295800-4297600 Enhancers Rectal Smooth Muscle rectum
14 chr7:4296000-4296200 Active TSS Stomach Smooth Muscle stomach
15 chr7:4296000-4296800 Enhancers Brain Germinal Matrix brain
16 chr7:4296000-4296800 Enhancers Fetal Kidney kidney
17 chr7:4296000-4297000 Enhancers Brain Cingulate Gyrus brain
18 chr7:4296000-4297000 Enhancers Fetal Brain Female brain

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