Variant report

Variant rs766163
Chromosome Location chr9:117200532-117200533
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117187000-117213800 Weak transcription Thymus Thymus
2 chr9:117189000-117215200 Weak transcription Fetal Intestine Small intestine
3 chr9:117193400-117200600 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr9:117196600-117208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:117197600-117202600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr9:117198000-117201400 Weak transcription Brain Cingulate Gyrus brain
7 chr9:117198000-117204200 Weak transcription Ovary ovary
8 chr9:117198400-117202800 Weak transcription Brain Hippocampus Middle brain
9 chr9:117198400-117203200 Weak transcription Brain Anterior Caudate brain
10 chr9:117198600-117201600 Weak transcription Brain Inferior Temporal Lobe brain
11 chr9:117198600-117203000 Weak transcription Brain Angular Gyrus brain
12 chr9:117198600-117204000 Weak transcription Fetal Lung lung
13 chr9:117198600-117208400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr9:117199800-117200600 Enhancers Brain Substantia Nigra brain
15 chr9:117199800-117200600 Enhancers Pancreas Pancrea
16 chr9:117199800-117200600 Enhancers K562 blood
17 chr9:117200400-117204400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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