Variant report

Variant rs73687963
Chromosome Location chr7:41263512-41263513
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41259400-41263800 Weak transcription NH-A brain
2 chr7:41259400-41278400 Weak transcription HSMM muscle
3 chr7:41260800-41264800 Enhancers Hela-S3 cervix
4 chr7:41261600-41265600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:41261800-41264600 Enhancers Muscle Satellite Cultured Cells --
6 chr7:41261800-41265800 Enhancers HMEC breast
7 chr7:41262200-41265600 Enhancers NHEK skin
8 chr7:41262400-41265600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr7:41262800-41263800 Weak transcription NHDF-Ad bronchial
10 chr7:41262800-41264600 Weak transcription Esophagus oesophagus
11 chr7:41263000-41263600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr7:41263200-41263600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr7:41263200-41264400 Weak transcription Placenta Placenta
14 chr7:41263400-41263800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr7:41263400-41264800 Enhancers HUVEC blood vessel

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