Variant report

Variant rs12129080
Chromosome Location chr1:94213146-94213147
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94199400-94217400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94208200-94215600 Weak transcription Aorta Aorta
3 chr1:94210800-94215600 Weak transcription Thymus Thymus
4 chr1:94211800-94215600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:94212400-94213200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:94212400-94213200 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:94212400-94214400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:94212600-94213200 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:94212600-94213200 ZNF genes & repeats NHEK skin
10 chr1:94212600-94213400 ZNF genes & repeats HMEC breast
11 chr1:94212600-94215200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:94212600-94217200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:94213000-94216200 Weak transcription Esophagus oesophagus

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