Variant report

Variant rs1105697
Chromosome Location chr7:4240699-4240700
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr7:4240200-4240800 ZNF genes & repeats Spleen Spleen
12 chr7:4240200-4241600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr7:4240400-4241000 Enhancers NHEK skin
14 chr7:4240400-4241800 Weak transcription Fetal Muscle Leg muscle
15 chr7:4240400-4242000 Enhancers Skeletal Muscle Female skeletal muscle
16 chr7:4240400-4243400 Weak transcription Fetal Lung lung
17 chr7:4240600-4241000 Enhancers Skeletal Muscle Male skeletal muscle

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