Variant report

Variant rs1265279
Chromosome Location chr6:4467156-4467157
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4460000-4472400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:4462400-4469400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr6:4465600-4467400 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr6:4466200-4467200 Enhancers HUVEC blood vessel
5 chr6:4466200-4467600 Enhancers Cortex derived primary cultured neurospheres brain
6 chr6:4466400-4467200 Enhancers Brain Hippocampus Middle brain
7 chr6:4466400-4467200 Enhancers Brain Substantia Nigra brain
8 chr6:4466400-4467400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr6:4466400-4467400 Enhancers Brain Angular Gyrus brain
10 chr6:4466400-4467600 Enhancers Brain Inferior Temporal Lobe brain
11 chr6:4466400-4468000 Enhancers Placenta Placenta
12 chr6:4466600-4467400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr6:4466600-4467400 Enhancers Brain Cingulate Gyrus brain
14 chr6:4466800-4471000 Weak transcription H1 Cell Line embryonic stem cell
15 chr6:4466800-4472400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr6:4467000-4467400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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