Variant report

Variant rs10148527
Chromosome Location chr14:68368055-68368056
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68364200-68374000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
2 chr14:68364400-68368400 Weak transcription Primary T regulatory cells fromperipheralblood blood
3 chr14:68365800-68374800 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr14:68367000-68368200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
5 chr14:68367400-68368200 ZNF genes & repeats Primary hematopoietic stem cells blood
6 chr14:68367600-68368400 ZNF genes & repeats Primary B cells from cord blood blood
7 chr14:68367600-68368400 ZNF genes & repeats Primary T cells from cord blood blood
8 chr14:68367800-68368200 ZNF genes & repeats Ovary ovary
9 chr14:68367800-68368400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr14:68367800-68368400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr14:68367800-68368600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr14:68367800-68368600 ZNF genes & repeats Dnd41 blood
13 chr14:68367800-68368800 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
14 chr14:68368000-68370600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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