Variant report

Variant rs35299722
Chromosome Location chr8:129868421-129868422
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129858600-129868800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:129864200-129873200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr8:129864200-129873200 Weak transcription NH-A brain
4 chr8:129864400-129873400 Weak transcription Muscle Satellite Cultured Cells --
5 chr8:129865600-129869000 Enhancers Cortex derived primary cultured neurospheres brain
6 chr8:129866200-129869200 Enhancers NHDF-Ad bronchial
7 chr8:129866400-129869200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr8:129866600-129869000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr8:129866600-129873200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr8:129866800-129868600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr8:129866800-129869000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr8:129866800-129869600 Weak transcription Dnd41 blood
13 chr8:129867200-129873200 Weak transcription Osteobl bone
14 chr8:129867800-129870600 Weak transcription H1 Cell Line embryonic stem cell
15 chr8:129868000-129868800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr8:129868000-129873000 Weak transcription iPS-15b Cell Line embryonic stem cell

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