Variant report

Variant rs2064957
Chromosome Location chr14:39337503-39337504
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:39334800-39339000 Enhancers Brain Cingulate Gyrus brain
2 chr14:39334800-39340000 Enhancers Brain Hippocampus Middle brain
3 chr14:39334800-39340200 Enhancers Brain Substantia Nigra brain
4 chr14:39335200-39337600 Weak transcription Pancreas Pancrea
5 chr14:39335600-39337600 Enhancers Fetal Intestine Small intestine
6 chr14:39336200-39337600 Weak transcription Fetal Intestine Large intestine
7 chr14:39336200-39338400 Weak transcription Rectal Mucosa Donor 29 rectum
8 chr14:39336600-39337800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr14:39336600-39339800 Enhancers Stomach Mucosa stomach
10 chr14:39336600-39340000 Enhancers Fetal Kidney kidney
11 chr14:39336800-39337600 Enhancers Liver Liver
12 chr14:39336800-39337600 Weak transcription Brain Anterior Caudate brain
13 chr14:39336800-39339200 Weak transcription Brain Inferior Temporal Lobe brain
14 chr14:39337000-39337600 Enhancers HepG2 liver
15 chr14:39337000-39338600 Enhancers Rectal Mucosa Donor 31 rectum
16 chr14:39337000-39342400 Weak transcription Primary neutrophils fromperipheralblood blood
17 chr14:39337200-39338400 Weak transcription Brain Angular Gyrus brain
18 chr14:39337400-39337600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
19 chr14:39337400-39339000 Enhancers Fetal Lung lung
20 chr14:39337400-39339000 Enhancers HUVEC blood vessel

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