Variant report

Variant rs4902532
Chromosome Location chr14:68365938-68365939
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68328000-68367800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr14:68334600-68367600 Weak transcription Primary B cells from cord blood blood
3 chr14:68351400-68367600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr14:68351400-68367800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr14:68351600-68367400 Weak transcription Primary hematopoietic stem cells blood
6 chr14:68352000-68367600 Weak transcription Primary T cells from cord blood blood
7 chr14:68364200-68374000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
8 chr14:68364400-68368400 Weak transcription Primary T regulatory cells fromperipheralblood blood
9 chr14:68365800-68374800 Weak transcription iPS-15b Cell Line embryonic stem cell

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