Variant report

Variant rs66705539
Chromosome Location chr2:48636432-48636433
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:48628200-48640000 Weak transcription Brain Inferior Temporal Lobe brain
2 chr2:48634000-48641400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr2:48634400-48641800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr2:48634600-48640200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:48634600-48641400 Weak transcription Duodenum Mucosa Duodenum
6 chr2:48634600-48642200 Weak transcription Small Intestine intestine
7 chr2:48635000-48640000 Weak transcription Fetal Intestine Large intestine
8 chr2:48635200-48640000 Weak transcription Fetal Intestine Small intestine
9 chr2:48635600-48641400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr2:48636200-48636600 Enhancers HUES64 Cell Line embryonic stem cell
11 chr2:48636200-48636800 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:48636200-48636800 Active TSS Hela-S3 cervix
13 chr2:48636200-48637000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:48636200-48637200 Active TSS A549 lung
15 chr2:48636400-48639400 Weak transcription NHDF-Ad bronchial
16 chr2:48636400-48640000 Enhancers Adipose Nuclei Adipose

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