Variant report

Variant rs2849402
Chromosome Location chr18:12046370-12046371
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:12039400-12047000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr18:12039400-12047400 Weak transcription Gastric stomach
3 chr18:12039400-12048400 Weak transcription Right Ventricle heart
4 chr18:12042000-12048600 Weak transcription HSMMtube muscle
5 chr18:12042800-12048200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr18:12045000-12048400 Weak transcription NH-A brain
7 chr18:12045600-12046600 Enhancers HMEC breast
8 chr18:12045600-12049000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr18:12045800-12046600 Enhancers Pancreas Pancrea
10 chr18:12045800-12047000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr18:12045800-12048400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr18:12045800-12048400 Weak transcription Osteobl bone
13 chr18:12046000-12046600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr18:12046200-12046400 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr18:12046200-12046600 Enhancers Esophagus oesophagus
16 chr18:12046200-12047000 Enhancers Lung lung
17 chr18:12046200-12048600 Weak transcription GM12878-XiMat blood

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