Variant report

Variant rs9415735
Chromosome Location chr10:52916964-52916965
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:52895200-52924000 Weak transcription Fetal Stomach stomach
2 chr10:52898000-52919600 Weak transcription NHLF lung
3 chr10:52906000-52931200 Weak transcription Fetal Muscle Leg muscle
4 chr10:52908000-52929600 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr10:52908400-52929600 Weak transcription Aorta Aorta
6 chr10:52910000-52931000 Weak transcription Fetal Lung lung
7 chr10:52910600-52942400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr10:52913000-52922000 Weak transcription Right Ventricle heart
9 chr10:52913200-52921800 Weak transcription Colon Smooth Muscle Colon
10 chr10:52916200-52917000 Enhancers Rectal Smooth Muscle rectum
11 chr10:52916600-52917000 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr10:52916600-52917000 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr10:52916600-52917200 Enhancers HUES48 Cell Line embryonic stem cell
14 chr10:52916800-52917000 Flanking Active TSS NHDF-Ad bronchial
15 chr10:52916800-52917200 Enhancers HUES64 Cell Line embryonic stem cell
16 chr10:52916800-52917200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr10:52916800-52917200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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