Variant report

Variant rs10895321
Chromosome Location chr11:102467291-102467292
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:102462200-102470000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:102463800-102469200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:102464000-102468800 Weak transcription HUVEC blood vessel
4 chr11:102464000-102469200 Weak transcription NHEK skin
5 chr11:102464000-102470800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:102464200-102469000 Weak transcription HMEC breast
7 chr11:102465200-102468600 Enhancers Fetal Intestine Large intestine
8 chr11:102465800-102467400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:102466000-102470600 Weak transcription Small Intestine intestine
10 chr11:102466800-102467600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr11:102466800-102474200 Enhancers HepG2 liver
12 chr11:102467000-102468200 Enhancers Fetal Intestine Small intestine
13 chr11:102467200-102470000 Enhancers A549 lung

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