Variant report

Variant rs11158641
Chromosome Location chr14:67102383-67102384
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67087000-67106800 Weak transcription Gastric stomach
2 chr14:67087200-67110000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr14:67095400-67116600 Weak transcription Brain Substantia Nigra brain
4 chr14:67095800-67112000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr14:67101000-67102400 Enhancers Fetal Heart heart
6 chr14:67101400-67105000 Weak transcription Right Atrium heart
7 chr14:67101400-67119600 Weak transcription Aorta Aorta
8 chr14:67101600-67102400 Enhancers Stomach Mucosa stomach
9 chr14:67101600-67102400 Enhancers NH-A brain
10 chr14:67101600-67102600 Enhancers HUVEC blood vessel
11 chr14:67101800-67102400 Enhancers Duodenum Smooth Muscle Duodenum
12 chr14:67101800-67109800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr14:67102000-67107800 Weak transcription Psoas Muscle Psoas
14 chr14:67102000-67110200 Weak transcription Liver Liver
15 chr14:67102000-67119400 Weak transcription Pancreas Pancrea
16 chr14:67102200-67102400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr14:67102200-67102400 Enhancers Fetal Lung lung
18 chr14:67102200-67105000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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