Variant report

Variant rs144619140
Chromosome Location chr17:16723076-16723077
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16716600-16723200 Weak transcription Right Atrium heart
2 chr17:16719000-16723200 Weak transcription Spleen Spleen
3 chr17:16719000-16724000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr17:16719200-16723600 Weak transcription NHEK skin
5 chr17:16720600-16723200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr17:16721400-16724600 Enhancers Adipose Nuclei Adipose
7 chr17:16721600-16723800 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr17:16722000-16723200 Enhancers Skeletal Muscle Male skeletal muscle
9 chr17:16722000-16724800 Enhancers Right Ventricle heart
10 chr17:16722200-16724200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr17:16722400-16723400 Enhancers Skeletal Muscle Female skeletal muscle
12 chr17:16722600-16723200 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr17:16722600-16724400 Enhancers Rectal Smooth Muscle rectum
14 chr17:16722600-16724600 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr17:16722600-16724800 Enhancers Left Ventricle heart
16 chr17:16722800-16723400 Bivalent Enhancer Stomach Smooth Muscle stomach
17 chr17:16722800-16723800 Enhancers HMEC breast
18 chr17:16722800-16724000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
19 chr17:16722800-16725200 Transcr. at gene 5' and 3' Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr17:16722800-16725200 Enhancers Esophagus oesophagus
21 chr17:16723000-16723600 Weak transcription Placenta Amnion Placenta Amnion
22 chr17:16723000-16724800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
23 chr17:16723000-16724800 Enhancers Fetal Heart heart
24 chr17:16723000-16725200 Enhancers Fetal Muscle Leg muscle

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