Variant report

Variant rs17166427
Chromosome Location chr7:7363349-7363350
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7360200-7364600 Enhancers Fetal Intestine Large intestine
2 chr7:7360400-7364400 Enhancers Fetal Intestine Small intestine
3 chr7:7361000-7363600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr7:7361000-7363800 Enhancers Primary B cells from peripheral blood blood
5 chr7:7361600-7366000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr7:7361800-7366400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:7361800-7367200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr7:7362000-7363800 Enhancers GM12878-XiMat blood
9 chr7:7362200-7363400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr7:7362200-7363800 Weak transcription Placenta Placenta
11 chr7:7362200-7366200 Weak transcription NHEK skin
12 chr7:7363000-7363600 Enhancers HUES6 Cell Line embryonic stem cell
13 chr7:7363000-7363600 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr7:7363000-7363800 Enhancers Fetal Kidney kidney
15 chr7:7363200-7363800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr7:7363200-7364200 Enhancers Spleen Spleen
17 chr7:7363200-7364400 Enhancers Gastric stomach
18 chr7:7363200-7364600 Enhancers Esophagus oesophagus

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