Variant report

Variant rs11051347
Chromosome Location chr12:31381140-31381141
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31373400-31386400 Enhancers Fetal Muscle Leg muscle
2 chr12:31375000-31381600 Weak transcription Gastric stomach
3 chr12:31376800-31384400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr12:31377200-31381800 Enhancers Fetal Muscle Trunk muscle
5 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr12:31379200-31383600 Enhancers Adipose Nuclei Adipose
7 chr12:31379800-31381200 Enhancers Spleen Spleen
8 chr12:31380000-31381200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr12:31380200-31382000 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr12:31380200-31382800 Enhancers Skeletal Muscle Male skeletal muscle
11 chr12:31380200-31383200 Enhancers Pancreas Pancrea
12 chr12:31380400-31381200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr12:31380400-31382400 Weak transcription Esophagus oesophagus
14 chr12:31380600-31382200 Weak transcription Psoas Muscle Psoas
15 chr12:31380800-31381800 Weak transcription Brain Germinal Matrix brain
16 chr12:31380800-31382600 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr12:31381000-31382000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
18 chr12:31381000-31382000 Weak transcription Cortex derived primary cultured neurospheres brain
19 chr12:31381000-31384000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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