Variant report

Variant rs17011265
Chromosome Location chr2:31525400-31525401
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31520400-31525800 Weak transcription Fetal Muscle Trunk muscle
2 chr2:31520600-31525800 Weak transcription Stomach Smooth Muscle stomach
3 chr2:31520600-31526000 Weak transcription Lung lung
4 chr2:31521000-31526400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:31521000-31526400 Weak transcription Right Ventricle heart
6 chr2:31521000-31527200 Weak transcription Aorta Aorta
7 chr2:31522600-31528600 Weak transcription Fetal Intestine Small intestine
8 chr2:31522800-31527800 Enhancers Fetal Heart heart
9 chr2:31522800-31528200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr2:31523800-31525800 Weak transcription NHEK skin
11 chr2:31524000-31525600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:31524000-31525800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:31524000-31525800 Weak transcription HMEC breast
14 chr2:31524000-31526000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr2:31525000-31527000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr2:31525000-31527400 Enhancers Left Ventricle heart
17 chr2:31525000-31527600 Enhancers Fetal Lung lung
18 chr2:31525200-31525600 Weak transcription Esophagus oesophagus
19 chr2:31525400-31527400 Enhancers Fetal Muscle Leg muscle

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