Variant report

Variant rs2870921
Chromosome Location chr12:67290739-67290740
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:67258000-67292600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:67279000-67292600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:67279600-67294400 Weak transcription H9 Cell Line embryonic stem cell
4 chr12:67284400-67292200 Weak transcription Primary T cells from cord blood blood
5 chr12:67289800-67291400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr12:67289800-67294000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr12:67290000-67290800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr12:67290400-67290800 Enhancers Colon Smooth Muscle Colon
9 chr12:67290400-67293400 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr12:67290400-67293600 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr12:67290600-67290800 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr12:67290600-67291000 Enhancers H1 Cell Line embryonic stem cell
13 chr12:67290600-67291200 Enhancers Fetal Brain Male brain
14 chr12:67290600-67292600 Weak transcription iPS-20b Cell Line embryonic stem cell

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