Variant report

Variant rs59531770
Chromosome Location chr12:31381939-31381940
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31373400-31386400 Enhancers Fetal Muscle Leg muscle
2 chr12:31376800-31384400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr12:31379200-31383600 Enhancers Adipose Nuclei Adipose
5 chr12:31380200-31382000 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr12:31380200-31382800 Enhancers Skeletal Muscle Male skeletal muscle
7 chr12:31380200-31383200 Enhancers Pancreas Pancrea
8 chr12:31380400-31382400 Weak transcription Esophagus oesophagus
9 chr12:31380600-31382200 Weak transcription Psoas Muscle Psoas
10 chr12:31380800-31382600 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr12:31381000-31382000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr12:31381000-31382000 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr12:31381000-31384000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr12:31381600-31382200 Enhancers Gastric stomach
15 chr12:31381800-31382200 Enhancers Liver Liver
16 chr12:31381800-31382400 Enhancers Brain Germinal Matrix brain
17 chr12:31381800-31382600 Bivalent Enhancer Fetal Muscle Trunk muscle
18 chr12:31381800-31382800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
19 chr12:31381800-31383200 Enhancers Fetal Intestine Large intestine
20 chr12:31381800-31383600 Enhancers Fetal Intestine Small intestine

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