Variant report

Variant rs117024434
Chromosome Location chr14:37643627-37643628
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37641800-37644200 Active TSS Right Atrium heart
2 chr14:37642400-37643800 Enhancers Fetal Heart heart
3 chr14:37642400-37644800 Weak transcription Pancreas Pancrea
4 chr14:37642400-37644800 Weak transcription Psoas Muscle Psoas
5 chr14:37642400-37645600 Weak transcription Fetal Intestine Small intestine
6 chr14:37642600-37643800 Enhancers HepG2 liver
7 chr14:37642600-37644600 Weak transcription A549 lung
8 chr14:37642600-37645200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr14:37642600-37645400 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr14:37642800-37643800 Weak transcription Colon Smooth Muscle Colon
11 chr14:37642800-37644800 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr14:37643000-37643800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr14:37643000-37643800 Weak transcription Liver Liver
14 chr14:37643400-37643800 Enhancers Brain Anterior Caudate brain
15 chr14:37643400-37643800 Enhancers Brain Hippocampus Middle brain
16 chr14:37643400-37644400 Weak transcription Skeletal Muscle Male skeletal muscle
17 chr14:37643600-37643800 Enhancers Stomach Mucosa stomach
18 chr14:37643600-37643800 Active TSS K562 blood

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