Variant report

Variant rs117815997
Chromosome Location chr8:8131331-8131332
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8120800-8131400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr8:8128400-8140800 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr8:8128600-8131600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr8:8128800-8131600 Weak transcription NHEK skin
5 chr8:8128800-8131800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr8:8128800-8131800 Weak transcription HMEC breast
7 chr8:8128800-8132000 Weak transcription Osteobl bone
8 chr8:8128800-8132600 Enhancers A549 lung
9 chr8:8128800-8142600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:8130400-8132000 Enhancers Ovary ovary
11 chr8:8130600-8133000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr8:8131000-8131400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr8:8131000-8132000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr8:8131200-8131400 Enhancers Placenta Amnion Placenta Amnion
15 chr8:8131200-8131400 Enhancers HepG2 liver
16 chr8:8131200-8131600 Weak transcription GM12878-XiMat blood

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