Variant report

Variant rs17229048
Chromosome Location chr15:33291862-33291863
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:33273200-33294000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr15:33286000-33294000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr15:33286800-33300000 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr15:33286800-33301200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr15:33287200-33294000 Weak transcription Osteobl bone
6 chr15:33287200-33300400 Weak transcription NHDF-Ad bronchial
7 chr15:33288800-33309200 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr15:33289200-33298800 Weak transcription Fetal Thymus thymus
9 chr15:33289400-33299400 Weak transcription NHLF lung
10 chr15:33289800-33292200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr15:33290200-33292000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr15:33291000-33299200 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr15:33291200-33301200 Weak transcription Sigmoid Colon Sigmoid Colon
14 chr15:33291400-33292000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr15:33291400-33292400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr15:33291400-33292400 Enhancers Adipose Nuclei Adipose
17 chr15:33291800-33292400 ZNF genes & repeats HSMM muscle

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