Variant report

Variant rs1792587
Chromosome Location chr11:15200492-15200493
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:15191000-15201000 Weak transcription Aorta Aorta
2 chr11:15197600-15200800 Enhancers Stomach Mucosa stomach
3 chr11:15197600-15201000 Weak transcription Fetal Muscle Trunk muscle
4 chr11:15197600-15201200 Weak transcription Gastric stomach
5 chr11:15197600-15211600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:15197800-15200600 Weak transcription Muscle Satellite Cultured Cells --
7 chr11:15197800-15221000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr11:15198600-15201400 Weak transcription Fetal Intestine Small intestine
9 chr11:15199000-15203200 Genic enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr11:15199400-15201400 Enhancers Primary neutrophils fromperipheralblood blood
11 chr11:15199800-15201600 Enhancers NHLF lung
12 chr11:15200000-15201000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr11:15200000-15201000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr11:15200000-15201400 Enhancers Fetal Muscle Leg muscle
15 chr11:15200000-15202600 Enhancers NHDF-Ad bronchial
16 chr11:15200200-15201400 Enhancers HSMMtube muscle
17 chr11:15200200-15202000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
18 chr11:15200200-15202200 Enhancers HSMM muscle
19 chr11:15200400-15201400 Enhancers Osteobl bone
20 chr11:15200400-15202600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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