Variant report

Variant rs9877865
Chromosome Location chr3:100421886-100421887
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr3:100417000-100423600 Weak transcription Esophagus oesophagus
3 chr3:100418800-100425000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr3:100420400-100422200 Enhancers K562 blood
5 chr3:100421400-100422000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr3:100421400-100422000 Enhancers Liver Liver
7 chr3:100421400-100422200 Enhancers Fetal Intestine Large intestine
8 chr3:100421400-100422200 Enhancers A549 lung
9 chr3:100421600-100422000 Weak transcription Fetal Intestine Small intestine
10 chr3:100421600-100422200 Enhancers GM12878-XiMat blood
11 chr3:100421600-100424800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr3:100421600-100424800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr3:100421600-100424800 Weak transcription HMEC breast
14 chr3:100421600-100424800 Weak transcription NHEK skin

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