Variant report

Variant rs375210143
Chromosome Location chr7:4235937-4235938
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr7:4230400-4237200 Weak transcription Fetal Intestine Small intestine
6 chr7:4230600-4242600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr7:4231000-4239800 Weak transcription Fetal Stomach stomach
8 chr7:4231200-4238600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr7:4231600-4239800 Weak transcription Right Atrium heart
10 chr7:4233000-4236600 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr7:4234800-4236800 Enhancers Esophagus oesophagus
12 chr7:4235000-4236000 Enhancers Fetal Muscle Leg muscle
13 chr7:4235000-4236200 Enhancers Fetal Muscle Trunk muscle
14 chr7:4235200-4236000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr7:4235400-4236400 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr7:4235600-4236000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr7:4235600-4240200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr7:4235800-4236400 Enhancers Spleen Spleen
19 chr7:4235800-4287200 Weak transcription Gastric stomach

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