Variant report

Variant rs4978586
Chromosome Location chr9:117192230-117192231
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117160800-117197000 Weak transcription Gastric stomach
2 chr9:117161200-117199200 Weak transcription Right Atrium heart
3 chr9:117175400-117196000 Weak transcription HepG2 liver
4 chr9:117180000-117193600 Weak transcription Brain Angular Gyrus brain
5 chr9:117180800-117192800 Weak transcription Lung lung
6 chr9:117181600-117196200 Weak transcription Pancreas Pancrea
7 chr9:117185800-117197000 Weak transcription Brain Inferior Temporal Lobe brain
8 chr9:117186400-117197200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr9:117186800-117193200 Weak transcription Brain Cingulate Gyrus brain
10 chr9:117187000-117213800 Weak transcription Thymus Thymus
11 chr9:117187400-117197000 Weak transcription Brain Anterior Caudate brain
12 chr9:117188600-117197200 Weak transcription Ovary ovary
13 chr9:117188600-117197800 Weak transcription Fetal Stomach stomach
14 chr9:117189000-117192800 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr9:117189000-117196200 Weak transcription Stomach Smooth Muscle stomach
16 chr9:117189000-117215200 Weak transcription Fetal Intestine Small intestine
17 chr9:117190200-117193000 Weak transcription Fetal Adrenal Gland Adrenal Gland
18 chr9:117190200-117196000 Weak transcription Spleen Spleen
19 chr9:117190200-117197400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
20 chr9:117191200-117197400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
21 chr9:117191800-117192600 Enhancers Brain Hippocampus Middle brain
22 chr9:117192000-117192400 Enhancers Brain Substantia Nigra brain
23 chr9:117192200-117193600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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