Variant report

Variant rs59379268
Chromosome Location chr1:186125204-186125205
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:186046400-186135200 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr1:186113800-186135800 Weak transcription Ovary ovary
3 chr1:186114600-186160800 Weak transcription Fetal Kidney kidney
4 chr1:186115400-186135400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:186116400-186135400 Weak transcription Aorta Aorta
6 chr1:186116600-186135400 Weak transcription Lung lung
7 chr1:186117200-186135800 Weak transcription Fetal Lung lung
8 chr1:186120000-186135200 Weak transcription Liver Liver
9 chr1:186120800-186125800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:186122200-186125600 Enhancers HMEC breast
11 chr1:186122200-186135600 Weak transcription K562 blood
12 chr1:186123000-186125800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:186123800-186134000 Weak transcription Adipose Nuclei Adipose
14 chr1:186124000-186125800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr1:186124200-186126200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr1:186124400-186125800 Enhancers NH-A brain
17 chr1:186124600-186125800 Enhancers NHEK skin
18 chr1:186124800-186125600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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