Variant report

Variant rs10132127
Chromosome Location chr14:104461494-104461495
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104456000-104465200 Strong transcription Monocytes-CD14+_RO01746 blood
2 chr14:104456400-104471600 Weak transcription Primary neutrophils fromperipheralblood blood
3 chr14:104456600-104470000 Weak transcription Pancreas Pancrea
4 chr14:104456600-104471400 Weak transcription Primary monocytes fromperipheralblood blood
5 chr14:104457000-104476400 Weak transcription Spleen Spleen
6 chr14:104460600-104461800 Weak transcription Placenta Amnion Placenta Amnion
7 chr14:104460600-104461800 Enhancers A549 lung
8 chr14:104460600-104461800 Enhancers NHEK skin
9 chr14:104461000-104461600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr14:104461200-104461600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr14:104461200-104462000 Enhancers HUES6 Cell Line embryonic stem cell
12 chr14:104461200-104462400 Enhancers HMEC breast
13 chr14:104461200-104462600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr14:104461400-104461800 Enhancers HUES64 Cell Line embryonic stem cell
15 chr14:104461400-104462200 Enhancers ES-I3 Cell Line embryonic stem cell

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