Variant report

Variant rs56258557
Chromosome Location chr7:17032337-17032338
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17020800-17033000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr7:17030000-17038000 Weak transcription Fetal Heart heart
3 chr7:17030000-17038400 Weak transcription Esophagus oesophagus
4 chr7:17030200-17034400 Weak transcription HSMMtube muscle
5 chr7:17030400-17032600 Active TSS Liver Liver
6 chr7:17030600-17033400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr7:17030600-17033800 Enhancers Placenta Placenta
8 chr7:17031000-17032600 Weak transcription Brain Substantia Nigra brain
9 chr7:17031000-17033600 Enhancers HepG2 liver
10 chr7:17031000-17035400 Weak transcription Brain Inferior Temporal Lobe brain
11 chr7:17031200-17047400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:17031400-17032400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr7:17031400-17032800 Weak transcription NHDF-Ad bronchial
14 chr7:17031400-17034000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr7:17031600-17033000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr7:17032200-17032400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr7:17032200-17033400 Enhancers Brain Cingulate Gyrus brain

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