Variant report

Variant rs10263742
Chromosome Location chr7:121435532-121435533
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121426600-121436200 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr7:121433800-121442400 Enhancers HMEC breast
3 chr7:121434000-121440200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr7:121434000-121440200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:121435000-121436000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr7:121435000-121436400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr7:121435000-121436800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:121435000-121437600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr7:121435000-121438400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr7:121435200-121436000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr7:121435200-121436600 Enhancers Fetal Brain Female brain
12 chr7:121435200-121437600 Enhancers Brain Germinal Matrix brain
13 chr7:121435400-121435800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:121435400-121435800 Enhancers Brain Hippocampus Middle brain
15 chr7:121435400-121435800 Flanking Active TSS NHEK skin
16 chr7:121435400-121436200 Enhancers Brain Substantia Nigra brain
17 chr7:121435400-121438800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
18 chr7:121435400-121440000 Enhancers H1 Cell Line embryonic stem cell

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