Variant report

Variant rs6958682
Chromosome Location chr7:4096689-4096690
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4082800-4097000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr7:4087600-4111800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr7:4088800-4129400 Weak transcription Right Ventricle heart
4 chr7:4093200-4104400 Weak transcription Fetal Stomach stomach
5 chr7:4093800-4097800 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr7:4095200-4104800 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr7:4096000-4116400 Weak transcription Adipose Nuclei Adipose
8 chr7:4096200-4097000 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:4096200-4097400 Strong transcription Fetal Intestine Small intestine
10 chr7:4096400-4097000 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr7:4096400-4097400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr7:4096400-4097400 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
13 chr7:4096400-4097400 ZNF genes & repeats Pancreas Pancrea
14 chr7:4096600-4096800 Weak transcription Spleen Spleen
15 chr7:4096600-4097200 Strong transcription Gastric stomach
16 chr7:4096600-4097200 ZNF genes & repeats Lung lung
17 chr7:4096600-4097400 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived
18 chr7:4096600-4097400 ZNF genes & repeats Aorta Aorta
19 chr7:4096600-4097400 Strong transcription Fetal Lung lung

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