Variant report

Variant rs745990
Chromosome Location chr18:11502296-11502297
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:11493800-11502400 Enhancers HSMM muscle
2 chr18:11493800-11502600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr18:11493800-11502600 Enhancers NHDF-Ad bronchial
4 chr18:11496400-11502800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr18:11496800-11502400 Enhancers NHLF lung
6 chr18:11497600-11502600 Enhancers HMEC breast
7 chr18:11498600-11502600 Enhancers HSMMtube muscle
8 chr18:11499600-11502800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr18:11500200-11506600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr18:11500600-11502600 Enhancers NH-A brain
11 chr18:11501000-11505800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr18:11501200-11502600 Enhancers Skeletal Muscle Female skeletal muscle
13 chr18:11501400-11502400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr18:11501400-11502600 Enhancers A549 lung
15 chr18:11501600-11504000 Enhancers HepG2 liver
16 chr18:11501800-11502400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr18:11502000-11506400 Weak transcription Hela-S3 cervix
18 chr18:11502200-11502600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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