Variant report

Variant rs145303663
Chromosome Location chr7:17133663-17133664
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17128200-17134600 Weak transcription Pancreas Pancrea
2 chr7:17129800-17133800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:17130400-17136600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr7:17130800-17134600 Weak transcription A549 lung
5 chr7:17131000-17133800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr7:17131000-17134200 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr7:17131000-17134600 Weak transcription Muscle Satellite Cultured Cells --
8 chr7:17131000-17135000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr7:17131200-17133800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:17131200-17134000 Weak transcription Osteobl bone
11 chr7:17131200-17134200 Weak transcription NHDF-Ad bronchial
12 chr7:17131200-17134400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:17131200-17134400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr7:17131200-17134800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr7:17132200-17137400 Enhancers NHEK skin
16 chr7:17133400-17135400 Weak transcription Primary monocytes fromperipheralblood blood
17 chr7:17133400-17140000 Enhancers HMEC breast
18 chr7:17133600-17138800 Enhancers Hela-S3 cervix

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