Variant report

Variant rs980003
Chromosome Location chr1:173027619-173027620
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173022400-173031000 Weak transcription HUVEC blood vessel
2 chr1:173022600-173030600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:173025800-173030800 Weak transcription HMEC breast
4 chr1:173026000-173031400 Weak transcription Placenta Amnion Placenta Amnion
5 chr1:173026200-173030600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:173026200-173030600 Weak transcription NHEK skin
7 chr1:173027200-173028000 Enhancers Fetal Lung lung
8 chr1:173027400-173028800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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