Variant report

Variant rs72666145
Chromosome Location chr14:32818862-32818863
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32797200-32831600 Weak transcription Right Atrium heart
2 chr14:32802600-32819000 Weak transcription Fetal Brain Male brain
3 chr14:32803200-32821600 Weak transcription Fetal Brain Female brain
4 chr14:32814000-32827800 Weak transcription Brain Germinal Matrix brain
5 chr14:32814800-32824000 Weak transcription Aorta Aorta
6 chr14:32815000-32819000 Weak transcription GM12878-XiMat blood
7 chr14:32815000-32823600 Weak transcription Brain Anterior Caudate brain
8 chr14:32815000-32827000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr14:32815200-32823600 Weak transcription Brain Angular Gyrus brain
10 chr14:32815400-32821800 Weak transcription Brain Substantia Nigra brain
11 chr14:32815400-32825600 Weak transcription Brain Cingulate Gyrus brain
12 chr14:32817000-32824000 Weak transcription Gastric stomach
13 chr14:32818000-32819000 Enhancers HMEC breast
14 chr14:32818000-32819200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr14:32818000-32819200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr14:32818000-32819400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr14:32818000-32819400 Enhancers NHEK skin
18 chr14:32818200-32819000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr14:32818400-32823800 Weak transcription Brain Inferior Temporal Lobe brain

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