Variant report

Variant rs59978302
Chromosome Location chr12:85267527-85267528
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:85250000-85271400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:85251000-85303000 Weak transcription NHEK skin
3 chr12:85251800-85285400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr12:85253800-85271200 Weak transcription Brain Inferior Temporal Lobe brain
5 chr12:85254000-85276800 Weak transcription Fetal Brain Male brain
6 chr12:85254000-85289800 Weak transcription Brain Angular Gyrus brain
7 chr12:85254600-85270600 Weak transcription Brain Substantia Nigra brain
8 chr12:85254800-85271200 Weak transcription Brain Hippocampus Middle brain
9 chr12:85255400-85284200 Weak transcription Brain Cingulate Gyrus brain
10 chr12:85257200-85268000 Weak transcription Hela-S3 cervix
11 chr12:85257400-85268800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr12:85258400-85268600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr12:85262000-85269200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr12:85263600-85268200 Strong transcription HMEC breast
15 chr12:85265800-85268200 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr12:85267200-85273800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr12:85267200-85274400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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