Variant report

Variant rs17035401
Chromosome Location chr12:104763044-104763045
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104749000-104763200 Weak transcription Primary T cells from cord blood blood
2 chr12:104749000-104765800 Weak transcription Thymus Thymus
3 chr12:104749200-104763400 Weak transcription HUVEC blood vessel
4 chr12:104749800-104769400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr12:104750400-104764800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr12:104753800-104765400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr12:104754400-104764800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr12:104757600-104765000 Weak transcription Aorta Aorta
9 chr12:104762000-104763200 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr12:104762000-104765000 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr12:104762800-104763400 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
12 chr12:104762800-104763800 ZNF genes & repeats H1 Cell Line embryonic stem cell
13 chr12:104762800-104763800 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
14 chr12:104763000-104763400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr12:104763000-104763600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr12:104763000-104763800 ZNF genes & repeats A549 lung

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