Variant report

Variant rs73678283
Chromosome Location chr8:49322869-49322870
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49318800-49323000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:49318800-49323000 Enhancers NHLF lung
3 chr8:49318800-49323200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr8:49319400-49323000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr8:49319800-49332400 Weak transcription Fetal Kidney kidney
6 chr8:49321000-49323400 Enhancers HMEC breast
7 chr8:49321600-49323200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr8:49321800-49323400 Enhancers HSMMtube muscle
9 chr8:49322000-49323600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr8:49322400-49323200 Enhancers NHEK skin
11 chr8:49322400-49323400 Enhancers Muscle Satellite Cultured Cells --
12 chr8:49322400-49323600 Enhancers HUVEC blood vessel
13 chr8:49322600-49323200 Enhancers NHDF-Ad bronchial
14 chr8:49322600-49323400 Enhancers HSMM muscle
15 chr8:49322600-49323600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr8:49322600-49323600 Enhancers Osteobl bone
17 chr8:49322800-49323000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr8:49322800-49323200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr8:49322800-49323200 Enhancers NH-A brain
20 chr8:49322800-49329800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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