Variant report

Variant rs59955258
Chromosome Location chr7:41264611-41264612
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41259400-41278400 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 chr7:41261800-41265800 Enhancers HMEC breast
5 chr7:41262200-41265600 Enhancers NHEK skin
6 chr7:41262400-41265600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:41263400-41264800 Enhancers HUVEC blood vessel
8 chr7:41263600-41264800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:41263800-41264800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr7:41263800-41265400 Enhancers Placenta Amnion Placenta Amnion
11 chr7:41264400-41265400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:41264400-41265800 Enhancers Placenta Placenta
13 chr7:41264600-41265000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr7:41264600-41265000 Enhancers Esophagus oesophagus
15 chr7:41264600-41265600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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