Variant report

Variant rs1745624
Chromosome Location chr1:78691290-78691291
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:78688000-78691400 Enhancers Hela-S3 cervix
2 chr1:78689400-78692200 Weak transcription Fetal Intestine Small intestine
3 chr1:78689600-78692800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:78689800-78692400 Enhancers Liver Liver
5 chr1:78689800-78697800 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr1:78689800-78702400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:78689800-78703000 Weak transcription Pancreas Pancrea
8 chr1:78690200-78691600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr1:78690200-78691600 Enhancers HUES64 Cell Line embryonic stem cell
10 chr1:78690200-78692600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:78690400-78691600 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:78690800-78691400 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr1:78690800-78691800 Weak transcription iPS-15b Cell Line embryonic stem cell
14 chr1:78690800-78693600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr1:78691000-78691800 Weak transcription Fetal Muscle Leg muscle
16 chr1:78691000-78692000 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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