Variant report

Variant rs80111519
Chromosome Location chr7:4063876-4063877
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4051200-4065600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr7:4053800-4065800 Weak transcription Fetal Brain Male brain
3 chr7:4054200-4065400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr7:4059000-4067000 Weak transcription Right Ventricle heart
5 chr7:4059000-4091200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr7:4059800-4065400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr7:4060200-4065000 Weak transcription Aorta Aorta
8 chr7:4061000-4065600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr7:4061400-4064200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr7:4061400-4067000 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr7:4061400-4073200 Weak transcription Fetal Lung lung
12 chr7:4061400-4080800 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr7:4061600-4064200 Weak transcription Spleen Spleen
14 chr7:4062400-4064800 Weak transcription Pancreas Pancrea
15 chr7:4062400-4065400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr7:4062800-4064000 Weak transcription H9 Cell Line embryonic stem cell
17 chr7:4062800-4065600 Weak transcription Fetal Muscle Trunk muscle
18 chr7:4063200-4065600 Weak transcription Fetal Muscle Leg muscle
19 chr7:4063400-4064800 Weak transcription Fetal Stomach stomach
20 chr7:4063400-4065400 Enhancers HepG2 liver

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