Variant report

Variant rs7782117
Chromosome Location chr7:17703728-17703729
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17699000-17703800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr7:17699800-17703800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:17700000-17703800 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr7:17701200-17703800 Enhancers NHLF lung
5 chr7:17702600-17703800 Enhancers Colon Smooth Muscle Colon
6 chr7:17702800-17703800 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr7:17702800-17704000 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr7:17702800-17704600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:17702800-17713800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr7:17703000-17704200 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr7:17703200-17704000 Enhancers NHDF-Ad bronchial
12 chr7:17703600-17704200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr7:17703600-17708800 Weak transcription NHEK skin
14 chr7:17703600-17713000 Weak transcription HMEC breast

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