Variant report

Variant rs570090606
Chromosome Location chr7:4098116-4098117
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4087600-4111800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr7:4088800-4129400 Weak transcription Right Ventricle heart
3 chr7:4093200-4104400 Weak transcription Fetal Stomach stomach
4 chr7:4095200-4104800 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr7:4096000-4116400 Weak transcription Adipose Nuclei Adipose
6 chr7:4096800-4098200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:4097200-4110000 Weak transcription Gastric stomach
8 chr7:4097400-4105800 Weak transcription Aorta Aorta
9 chr7:4097400-4106000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr7:4097400-4106800 Weak transcription Pancreas Pancrea
11 chr7:4097400-4108800 Weak transcription Fetal Intestine Small intestine
12 chr7:4097400-4109000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr7:4097400-4109400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
14 chr7:4097800-4098200 Enhancers Muscle Satellite Cultured Cells --

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