Variant report

Variant rs34041066
Chromosome Location chr7:17061148-17061149
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17050600-17071800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr7:17058800-17062800 Enhancers HepG2 liver
3 chr7:17059600-17063000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17059800-17062000 Enhancers Liver Liver
5 chr7:17059800-17062800 Enhancers HMEC breast
6 chr7:17060000-17061600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:17060000-17061600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr7:17060000-17061600 Enhancers NHEK skin
9 chr7:17060400-17061400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr7:17060600-17061200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr7:17060600-17061400 Weak transcription Fetal Intestine Small intestine
12 chr7:17060600-17061400 Weak transcription Stomach Mucosa stomach
13 chr7:17060800-17063800 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr7:17061000-17061200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:17061000-17061200 Enhancers NHDF-Ad bronchial
16 chr7:17061000-17061200 Enhancers Osteobl bone

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