Variant report

Variant rs4978588
Chromosome Location chr9:117197738-117197739
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117161200-117199200 Weak transcription Right Atrium heart
2 chr9:117187000-117213800 Weak transcription Thymus Thymus
3 chr9:117188600-117197800 Weak transcription Fetal Stomach stomach
4 chr9:117189000-117215200 Weak transcription Fetal Intestine Small intestine
5 chr9:117193400-117200600 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:117196600-117208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:117196800-117197800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr9:117196800-117198000 Enhancers Brain Cingulate Gyrus brain
9 chr9:117197000-117197800 Enhancers HUES6 Cell Line embryonic stem cell
10 chr9:117197000-117198000 Enhancers Brain Angular Gyrus brain
11 chr9:117197000-117198600 Enhancers Brain Inferior Temporal Lobe brain
12 chr9:117197200-117198000 Enhancers Ovary ovary
13 chr9:117197200-117198200 Enhancers Brain Substantia Nigra brain
14 chr9:117197400-117198400 Enhancers Brain Hippocampus Middle brain
15 chr9:117197400-117198600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr9:117197400-117199800 Weak transcription Pancreas Pancrea
17 chr9:117197600-117197800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
18 chr9:117197600-117197800 Enhancers Brain Anterior Caudate brain
19 chr9:117197600-117199000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
20 chr9:117197600-117199800 Weak transcription HepG2 liver
21 chr9:117197600-117202600 Weak transcription Breast Myoepithelial Primary Cells Breast

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