Variant report

Variant rs11989639
Chromosome Location chr8:129882921-129882922
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129874600-129886200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr8:129875000-129887000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:129876200-129886200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr8:129877000-129885000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr8:129881000-129886600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr8:129881400-129886400 Weak transcription NH-A brain
7 chr8:129881400-129886400 Weak transcription Osteobl bone
8 chr8:129881600-129885800 Weak transcription NHDF-Ad bronchial
9 chr8:129881600-129886600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:129881600-129894200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr8:129882800-129888600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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