Variant report

Variant rs16843893
Chromosome Location chr2:210741592-210741593
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210682000-210769600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
2 chr2:210733200-210791400 Weak transcription Brain Angular Gyrus brain
3 chr2:210735400-210769400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr2:210737800-210742800 Weak transcription Brain Cingulate Gyrus brain
5 chr2:210737800-210769400 Weak transcription Brain Anterior Caudate brain
6 chr2:210737800-210772400 Weak transcription Brain Inferior Temporal Lobe brain
7 chr2:210739400-210744200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:210739600-210742200 Enhancers NHEK skin
9 chr2:210739600-210744200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:210740200-210741600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:210740800-210742000 Enhancers Fetal Lung lung
12 chr2:210740800-210742600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:210741200-210742400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr2:210741200-210743000 Enhancers Cortex derived primary cultured neurospheres brain
15 chr2:210741400-210741600 Enhancers Fetal Brain Female brain

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