Variant report

Variant rs17154032
Chromosome Location chr8:8426601-8426602
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8422200-8432000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr8:8422400-8430200 Weak transcription Osteobl bone
3 chr8:8422600-8430600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr8:8423200-8430600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr8:8426000-8426800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:8426000-8427000 Flanking Active TSS GM12878-XiMat blood
7 chr8:8426200-8426800 Enhancers Rectal Smooth Muscle rectum
8 chr8:8426200-8427000 Enhancers Primary B cells from peripheral blood blood
9 chr8:8426400-8426800 Weak transcription Colon Smooth Muscle Colon
10 chr8:8426400-8426800 Enhancers Fetal Brain Male brain
11 chr8:8426400-8426800 Enhancers HepG2 liver
12 chr8:8426400-8427000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr8:8426400-8427200 Enhancers A549 lung
14 chr8:8426600-8426800 Enhancers Gastric stomach
15 chr8:8426600-8426800 Enhancers Lung lung
16 chr8:8426600-8428800 Strong transcription Breast Myoepithelial Primary Cells Breast
17 chr8:8426600-8430400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr8:8426600-8433000 Weak transcription Placenta Amnion Placenta Amnion

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