Variant report

Variant rs9659076
Chromosome Location chr1:246199147-246199148
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246193200-246202200 Weak transcription Aorta Aorta
2 chr1:246195800-246203000 Weak transcription Pancreas Pancrea
3 chr1:246196000-246207000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:246197800-246199600 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr1:246198400-246199800 Enhancers K562 blood
6 chr1:246198600-246199400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:246198800-246200400 Weak transcription Esophagus oesophagus
8 chr1:246199000-246199200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:246199000-246199200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:246199000-246199200 Enhancers Fetal Brain Male brain
11 chr1:246199000-246199200 Enhancers Stomach Smooth Muscle stomach
12 chr1:246199000-246199400 Enhancers Fetal Brain Female brain
13 chr1:246199000-246199400 Active TSS NHDF-Ad bronchial
14 chr1:246199000-246199600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr1:246199000-246199600 Enhancers Muscle Satellite Cultured Cells --
16 chr1:246199000-246199600 Enhancers Fetal Lung lung
17 chr1:246199000-246202800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr1:246199000-246221400 Weak transcription Osteobl bone

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