Variant report

Variant rs10236838
Chromosome Location chr7:4239852-4239853
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4229000-4240000 Weak transcription Fetal Lung lung
2 chr7:4229400-4244400 Weak transcription Stomach Smooth Muscle stomach
3 chr7:4229800-4268400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr7:4230000-4245600 Weak transcription Pancreas Pancrea
5 chr7:4230600-4242600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr7:4235600-4240200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:4235800-4287200 Weak transcription Gastric stomach
8 chr7:4236000-4240000 Weak transcription Fetal Muscle Leg muscle
9 chr7:4236200-4241400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr7:4239600-4240000 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
11 chr7:4239600-4240800 ZNF genes & repeats Fetal Intestine Small intestine
12 chr7:4239800-4241000 ZNF genes & repeats Esophagus oesophagus
13 chr7:4239800-4241000 ZNF genes & repeats Fetal Stomach stomach
14 chr7:4239800-4241200 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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