Variant report

Variant rs10172908
Chromosome Location chr2:134281355-134281356
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:134268200-134290000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:134274200-134281600 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:134279000-134281600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:134280600-134281600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
5 chr2:134280800-134281400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
6 chr2:134280800-134281400 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
7 chr2:134280800-134281400 Enhancers Ovary ovary
8 chr2:134280800-134281600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
9 chr2:134280800-134281600 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
10 chr2:134280800-134282400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr2:134281200-134281400 Bivalent Enhancer H9 Cell Line embryonic stem cell
12 chr2:134281200-134281400 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
13 chr2:134281200-134281400 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
14 chr2:134281200-134281400 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
15 chr2:134281200-134282600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived

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