Variant report

Variant rs59091698
Chromosome Location chr7:41263887-41263888
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41259400-41278400 Weak transcription HSMM muscle
2 chr7:41260800-41264800 Enhancers Hela-S3 cervix
3 chr7:41261600-41265600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:41261800-41264600 Enhancers Muscle Satellite Cultured Cells --
5 chr7:41261800-41265800 Enhancers HMEC breast
6 chr7:41262200-41265600 Enhancers NHEK skin
7 chr7:41262400-41265600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:41262800-41264600 Weak transcription Esophagus oesophagus
9 chr7:41263200-41264400 Weak transcription Placenta Placenta
10 chr7:41263400-41264800 Enhancers HUVEC blood vessel
11 chr7:41263600-41264400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:41263600-41264800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:41263800-41264400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr7:41263800-41264400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr7:41263800-41264400 Enhancers NHDF-Ad bronchial
16 chr7:41263800-41264400 Enhancers Osteobl bone
17 chr7:41263800-41264600 Enhancers NH-A brain
18 chr7:41263800-41264800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
19 chr7:41263800-41265400 Enhancers Placenta Amnion Placenta Amnion

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