Variant report

Variant rs1842771
Chromosome Location chr6:149135396-149135397
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:149115800-149144800 Weak transcription Primary B cells from cord blood blood
2 chr6:149125600-149136000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:149125800-149137000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:149128200-149135800 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr6:149128200-149136800 Weak transcription ES-WA7 Cell Line embryonic stem cell
6 chr6:149128800-149138000 Weak transcription Ovary ovary
7 chr6:149131200-149136400 Weak transcription H9 Cell Line embryonic stem cell
8 chr6:149133800-149137200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr6:149134800-149135600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr6:149135200-149135600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr6:149135200-149135600 Strong transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr6:149135200-149135600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:149135200-149135600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:149135200-149135600 Enhancers NHDF-Ad bronchial
15 chr6:149135200-149136400 ZNF genes & repeats H1 Cell Line embryonic stem cell

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