Variant report

Variant rs8007662
Chromosome Location chr14:67120432-67120433
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67117000-67121200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:67118600-67123000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr14:67119800-67121000 Weak transcription Aorta Aorta
4 chr14:67119800-67121000 Weak transcription Ovary ovary
5 chr14:67119800-67123600 Weak transcription Brain Substantia Nigra brain
6 chr14:67119800-67123800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr14:67120200-67120600 Weak transcription Psoas Muscle Psoas
8 chr14:67120400-67120600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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