Variant report

Variant rs9972348
Chromosome Location chr15:56185262-56185263
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:56166000-56185400 Weak transcription Hela-S3 cervix
2 chr15:56172000-56186200 Weak transcription Osteobl bone
3 chr15:56172800-56189600 Weak transcription Placenta Placenta
4 chr15:56175200-56186000 Weak transcription Muscle Satellite Cultured Cells --
5 chr15:56175400-56186200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr15:56175600-56186200 Weak transcription NHEK skin
7 chr15:56175800-56189400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr15:56176000-56216200 Weak transcription Fetal Intestine Small intestine
9 chr15:56176800-56186800 Weak transcription NH-A brain
10 chr15:56181600-56186400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr15:56181600-56186600 Weak transcription Primary hematopoietic stem cells blood
12 chr15:56181800-56186400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr15:56181800-56188800 Weak transcription HMEC breast
14 chr15:56184400-56186200 Weak transcription Psoas Muscle Psoas
15 chr15:56184800-56185400 Strong transcription HSMM muscle
16 chr15:56185000-56185600 Flanking Active TSS A549 lung
17 chr15:56185000-56186600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr15:56185000-56189600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
19 chr15:56185200-56187800 Active TSS Skeletal Muscle Male skeletal muscle

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