Variant report

Variant rs73059529
Chromosome Location chr1:184259591-184259592
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:184255600-184266400 Weak transcription Spleen Spleen
2 chr1:184256000-184266000 Weak transcription Right Atrium heart
3 chr1:184258000-184261600 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:184258600-184267400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:184258800-184259600 ZNF genes & repeats hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr1:184258800-184259800 Enhancers NHEK skin
7 chr1:184258800-184265200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:184259000-184259800 Enhancers HMEC breast
9 chr1:184259200-184259600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:184259200-184259600 ZNF genes & repeats A549 lung
11 chr1:184259400-184259600 ZNF genes & repeats Gastric stomach
12 chr1:184259400-184259600 Enhancers Pancreas Pancrea
13 chr1:184259400-184260400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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