Variant report

Variant rs535502033
Chromosome Location chr7:7344713-7344714
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr7:7341800-7344800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr7:7342800-7345000 Enhancers Placenta Placenta
4 chr7:7342800-7346000 Enhancers Esophagus oesophagus
5 chr7:7343000-7346400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr7:7343200-7346400 Enhancers Fetal Intestine Large intestine
7 chr7:7344200-7344800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr7:7344200-7346400 Enhancers Fetal Intestine Small intestine
9 chr7:7344400-7344800 Enhancers Gastric stomach
10 chr7:7344400-7345000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr7:7344400-7345000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr7:7344400-7345000 Enhancers NHEK skin

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