Variant report

Variant rs744664
Chromosome Location chr12:117732101-117732102
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:117697200-117746200 Weak transcription Brain Anterior Caudate brain
2 chr12:117728000-117771200 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr12:117728600-117732200 Weak transcription NHEK skin
4 chr12:117731600-117732600 Enhancers Brain Germinal Matrix brain
5 chr12:117731800-117732400 Enhancers HUES6 Cell Line embryonic stem cell
6 chr12:117731800-117732400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr12:117731800-117732800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr12:117732000-117732200 Bivalent Enhancer Fetal Brain Male brain
9 chr12:117732000-117732200 Bivalent Enhancer Fetal Brain Female brain
10 chr12:117732000-117732200 Bivalent Enhancer Fetal Stomach stomach
11 chr12:117732000-117732400 Enhancers H1 Cell Line embryonic stem cell
12 chr12:117732000-117732400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:117732000-117732400 Enhancers Esophagus oesophagus
14 chr12:117732000-117732600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr12:117732000-117732600 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr12:117732000-117732800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
17 chr12:117732000-117732800 Bivalent Enhancer Fetal Muscle Trunk muscle

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