Variant report

Variant rs11051342
Chromosome Location chr12:31380234-31380235
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr12:31375400-31380800 Enhancers Brain Germinal Matrix brain
4 chr12:31376800-31384400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr12:31377200-31381800 Enhancers Fetal Muscle Trunk muscle
6 chr12:31378400-31380400 Enhancers Esophagus oesophagus
7 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr12:31379200-31383600 Enhancers Adipose Nuclei Adipose
9 chr12:31379800-31381000 Enhancers Cortex derived primary cultured neurospheres brain
10 chr12:31379800-31381200 Enhancers Spleen Spleen
11 chr12:31380000-31380400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr12:31380000-31381200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr12:31380200-31380400 Bivalent Enhancer HepG2 liver
14 chr12:31380200-31380600 Enhancers Psoas Muscle Psoas
15 chr12:31380200-31380800 Enhancers Skeletal Muscle Female skeletal muscle
16 chr12:31380200-31382000 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr12:31380200-31382800 Enhancers Skeletal Muscle Male skeletal muscle
18 chr12:31380200-31383200 Enhancers Pancreas Pancrea

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