Variant report

Variant rs4362750
Chromosome Location chr3:110383886-110383887
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:110381400-110384000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr3:110381800-110389200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr3:110382200-110385200 Weak transcription Fetal Intestine Small intestine
4 chr3:110382600-110384000 Enhancers HUVEC blood vessel
5 chr3:110382600-110384200 Enhancers Muscle Satellite Cultured Cells --
6 chr3:110382800-110384000 Enhancers HSMM muscle
7 chr3:110382800-110384200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr3:110382800-110384400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr3:110383000-110384000 Enhancers NHDF-Ad bronchial
10 chr3:110383000-110384000 Enhancers Osteobl bone
11 chr3:110383200-110384000 Enhancers NHLF lung
12 chr3:110383200-110385800 Enhancers Stomach Mucosa stomach
13 chr3:110383600-110384000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr3:110383800-110384000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr3:110383800-110384000 Enhancers Fetal Lung lung
16 chr3:110383800-110384200 Enhancers Pancreas Pancrea
17 chr3:110383800-110384400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr3:110383800-110384400 Enhancers Gastric stomach

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