Variant report

Variant rs7863056
Chromosome Location chr9:117202395-117202396
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr9:117196600-117208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:117197600-117202600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr9:117198000-117204200 Weak transcription Ovary ovary
6 chr9:117198400-117202800 Weak transcription Brain Hippocampus Middle brain
7 chr9:117198400-117203200 Weak transcription Brain Anterior Caudate brain
8 chr9:117198600-117203000 Weak transcription Brain Angular Gyrus brain
9 chr9:117198600-117204000 Weak transcription Fetal Lung lung
10 chr9:117198600-117208400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr9:117200400-117204400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr9:117200600-117204800 Weak transcription Pancreas Pancrea
13 chr9:117200600-117208000 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr9:117201800-117203200 Weak transcription Brain Cingulate Gyrus brain
15 chr9:117202000-117203200 Weak transcription Brain Inferior Temporal Lobe brain
16 chr9:117202200-117202600 Weak transcription Brain Substantia Nigra brain

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