Variant report

Variant rs57916848
Chromosome Location chr6:13870879-13870880
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:13864400-13872600 Weak transcription Placenta Placenta
2 chr6:13865600-13873200 Weak transcription Fetal Intestine Small intestine
3 chr6:13867200-13872600 Weak transcription Primary monocytes fromperipheralblood blood
4 chr6:13867200-13872600 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr6:13868400-13873400 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr6:13869800-13871600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr6:13870400-13871200 Enhancers Adipose Nuclei Adipose
8 chr6:13870400-13871400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr6:13870600-13871000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr6:13870600-13871000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr6:13870600-13871000 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr6:13870600-13871000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
13 chr6:13870600-13871400 Enhancers Brain Cingulate Gyrus brain
14 chr6:13870600-13871400 Enhancers Fetal Muscle Leg muscle
15 chr6:13870800-13871200 Enhancers Fetal Brain Male brain
16 chr6:13870800-13873600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr6:13870800-13873600 Weak transcription Fetal Lung lung

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