Variant report

Variant rs35501796
Chromosome Location chr11:86964159-86964160
allele -/A
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86961400-86967800 Weak transcription NHDF-Ad bronchial
2 chr11:86962400-86972000 Weak transcription Primary T cells from cord blood blood
3 chr11:86962800-86977600 Weak transcription K562 blood
4 chr11:86963000-86976200 Weak transcription Colon Smooth Muscle Colon
5 chr11:86963200-86965800 Weak transcription Rectal Smooth Muscle rectum
6 chr11:86963200-86969400 Weak transcription Adipose Nuclei Adipose
7 chr11:86963600-86964400 Enhancers HUVEC blood vessel
8 chr11:86963800-86964400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:86963800-86964600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr11:86964000-86964200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:86964000-86964400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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