Variant report

Variant rs59286366
Chromosome Location chr8:129885933-129885934
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr8:129881000-129886600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:129881400-129886400 Weak transcription NH-A brain
6 chr8:129881400-129886400 Weak transcription Osteobl bone
7 chr8:129881600-129886600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr8:129881600-129894200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr8:129882800-129888600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr8:129884200-129886400 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr8:129885000-129887400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr8:129885600-129887400 Enhancers HUES64 Cell Line embryonic stem cell
13 chr8:129885800-129886000 Weak transcription HSMM muscle
14 chr8:129885800-129886400 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr8:129885800-129887400 Enhancers NHDF-Ad bronchial

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