Variant report

Variant rs12826616
Chromosome Location chr12:31379463-31379464
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31373200-31380200 Weak transcription Pancreas Pancrea
2 chr12:31373400-31386400 Enhancers Fetal Muscle Leg muscle
3 chr12:31375000-31381600 Weak transcription Gastric stomach
4 chr12:31375400-31380800 Enhancers Brain Germinal Matrix brain
5 chr12:31376800-31384400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr12:31377200-31379800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr12:31377200-31381800 Enhancers Fetal Muscle Trunk muscle
8 chr12:31377800-31380200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr12:31378200-31379800 Enhancers Placenta Amnion Placenta Amnion
10 chr12:31378400-31379800 Weak transcription Spleen Spleen
11 chr12:31378400-31380200 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr12:31378400-31380400 Enhancers Esophagus oesophagus
13 chr12:31378600-31379800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr12:31378600-31379800 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr12:31378600-31387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr12:31379200-31379800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
17 chr12:31379200-31383600 Enhancers Adipose Nuclei Adipose
18 chr12:31379400-31379800 Enhancers HSMMtube muscle

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