Variant report

Variant rs1105696
Chromosome Location chr7:4240387-4240388
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4229400-4244400 Weak transcription Stomach Smooth Muscle stomach
2 chr7:4229800-4268400 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr7:4230000-4245600 Weak transcription Pancreas Pancrea
4 chr7:4230600-4242600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr7:4235800-4287200 Weak transcription Gastric stomach
6 chr7:4236200-4241400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr7:4239600-4240800 ZNF genes & repeats Fetal Intestine Small intestine
8 chr7:4239800-4241000 ZNF genes & repeats Esophagus oesophagus
9 chr7:4239800-4241000 ZNF genes & repeats Fetal Stomach stomach
10 chr7:4239800-4241200 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr7:4240000-4240400 ZNF genes & repeats Fetal Lung lung
12 chr7:4240000-4240400 ZNF genes & repeats Fetal Muscle Leg muscle
13 chr7:4240200-4240800 ZNF genes & repeats Spleen Spleen
14 chr7:4240200-4241600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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