Variant report

Variant rs17166438
Chromosome Location chr7:7363777-7363778
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr7:7361000-7363800 Enhancers Primary B cells from peripheral blood blood
4 chr7:7361600-7366000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:7361800-7366400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:7361800-7367200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr7:7362000-7363800 Enhancers GM12878-XiMat blood
8 chr7:7362200-7363800 Weak transcription Placenta Placenta
9 chr7:7362200-7366200 Weak transcription NHEK skin
10 chr7:7363000-7363800 Enhancers Fetal Kidney kidney
11 chr7:7363200-7363800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr7:7363200-7364200 Enhancers Spleen Spleen
13 chr7:7363200-7364400 Enhancers Gastric stomach
14 chr7:7363200-7364600 Enhancers Esophagus oesophagus
15 chr7:7363400-7363800 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr7:7363600-7363800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr7:7363600-7366400 Weak transcription Breast Myoepithelial Primary Cells Breast

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