Variant report

Variant rs7861571
Chromosome Location chr9:110870097-110870098
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110858000-110870600 Weak transcription A549 lung
2 chr9:110863200-110881600 Weak transcription Gastric stomach
3 chr9:110866000-110870600 Weak transcription NHDF-Ad bronchial
4 chr9:110866200-110870800 Weak transcription Osteobl bone
5 chr9:110866400-110870600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr9:110866400-110871200 Weak transcription Fetal Stomach stomach
7 chr9:110867400-110880200 Weak transcription Esophagus oesophagus
8 chr9:110867600-110881600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:110868200-110870400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr9:110868400-110870400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:110868600-110870600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:110868600-110870600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr9:110868600-110870600 Weak transcription Stomach Mucosa stomach
14 chr9:110868600-110870800 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr9:110868600-110899800 Weak transcription H9 Cell Line embryonic stem cell
16 chr9:110868800-110871000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr9:110869800-110870400 Enhancers K562 blood

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