Variant report

Variant rs187939096
Chromosome Location chr12:10563799-10563800
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10548600-10564000 Weak transcription Brain Angular Gyrus brain
2 chr12:10550800-10564000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:10559800-10563800 Weak transcription Primary B cells from cord blood blood
4 chr12:10559800-10564000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:10562200-10563800 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr12:10562200-10563800 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr12:10562200-10564000 Weak transcription K562 blood
8 chr12:10562200-10566600 Weak transcription Hela-S3 cervix
9 chr12:10562200-10572800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr12:10562400-10563800 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr12:10562400-10563800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr12:10562400-10563800 Weak transcription Primary T killer naive cells fromperipheralblood blood
13 chr12:10563000-10564400 Transcr. at gene 5' and 3' Primary Natural Killer cells fromperipheralblood blood
14 chr12:10563600-10563800 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr12:10563600-10564200 Enhancers HUES48 Cell Line embryonic stem cell
16 chr12:10563600-10564600 Enhancers HUES64 Cell Line embryonic stem cell

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