Variant report

Variant rs188028436
Chromosome Location chr7:7344877-7344878
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7340800-7345000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:7342800-7345000 Enhancers Placenta Placenta
3 chr7:7342800-7346000 Enhancers Esophagus oesophagus
4 chr7:7343000-7346400 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr7:7343200-7346400 Enhancers Fetal Intestine Large intestine
6 chr7:7344200-7346400 Enhancers Fetal Intestine Small intestine
7 chr7:7344400-7345000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:7344400-7345000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr7:7344400-7345000 Enhancers NHEK skin
10 chr7:7344800-7345000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr7:7344800-7345600 Weak transcription Gastric stomach

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