Variant report

Variant rs8046259
Chromosome Location chr16:47814421-47814422
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:47813400-47814800 Enhancers iPS-15b Cell Line embryonic stem cell
2 chr16:47813400-47815000 Enhancers HUES48 Cell Line embryonic stem cell
3 chr16:47813400-47815200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr16:47813400-47815400 Enhancers H9 Cell Line embryonic stem cell
5 chr16:47813400-47815400 Enhancers HUES64 Cell Line embryonic stem cell
6 chr16:47813400-47816400 Enhancers Fetal Brain Male brain
7 chr16:47813600-47815600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr16:47813600-47818600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr16:47813800-47814600 Enhancers Spleen Spleen
10 chr16:47814000-47814600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr16:47814000-47814600 Enhancers NHDF-Ad bronchial
12 chr16:47814000-47814800 Enhancers GM12878-XiMat blood
13 chr16:47814200-47814600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr16:47814200-47814600 Enhancers Primary T helper naive cells from peripheral blood blood
15 chr16:47814200-47814600 Enhancers Cortex derived primary cultured neurospheres brain
16 chr16:47814400-47814600 Enhancers ES-I3 Cell Line embryonic stem cell
17 chr16:47814400-47815400 Enhancers H1 Cell Line embryonic stem cell

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