Variant report

Variant rs9261093
Chromosome Location chr6:29970685-29970686
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29964400-29974400 Weak transcription Hela-S3 cervix
2 chr6:29966800-29974000 Weak transcription Spleen Spleen
3 chr6:29970400-29970800 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr6:29970400-29970800 Enhancers NHDF-Ad bronchial
5 chr6:29970400-29971000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:29970400-29971000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:29970400-29971000 Enhancers NHEK skin
8 chr6:29970600-29970800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
9 chr6:29970600-29971000 Enhancers HMEC breast

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