Variant report

Variant rs10148659
Chromosome Location chr14:32820586-32820587
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32797200-32831600 Weak transcription Right Atrium heart
2 chr14:32803200-32821600 Weak transcription Fetal Brain Female brain
3 chr14:32814000-32827800 Weak transcription Brain Germinal Matrix brain
4 chr14:32814800-32824000 Weak transcription Aorta Aorta
5 chr14:32815000-32823600 Weak transcription Brain Anterior Caudate brain
6 chr14:32815000-32827000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
7 chr14:32815200-32823600 Weak transcription Brain Angular Gyrus brain
8 chr14:32815400-32821800 Weak transcription Brain Substantia Nigra brain
9 chr14:32815400-32825600 Weak transcription Brain Cingulate Gyrus brain
10 chr14:32817000-32824000 Weak transcription Gastric stomach
11 chr14:32818400-32823800 Weak transcription Brain Inferior Temporal Lobe brain
12 chr14:32819200-32834200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr14:32819400-32820600 Weak transcription NHEK skin
14 chr14:32819400-32820800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr14:32820400-32822400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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