Variant report

Variant rs74085976
Chromosome Location chr12:38531537-38531538
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:38529400-38532200 Weak transcription Hela-S3 cervix
2 chr12:38529800-38531800 Weak transcription A549 lung
3 chr12:38530600-38533000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:38531400-38531600 Active TSS ES-I3 Cell Line embryonic stem cell
5 chr12:38531400-38531600 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr12:38531400-38531600 Bivalent/Poised TSS Primary T helper naive cells fromperipheralblood blood
7 chr12:38531400-38531600 Bivalent/Poised TSS Primary T killer naive cells fromperipheralblood blood
8 chr12:38531400-38531600 Bivalent/Poised TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr12:38531400-38531600 ZNF genes & repeats Gastric stomach
10 chr12:38531400-38531600 Flanking Bivalent TSS/Enh Stomach Mucosa stomach
11 chr12:38531400-38531800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
12 chr12:38531400-38531800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
13 chr12:38531400-38531800 Bivalent Enhancer Brain Cingulate Gyrus brain
14 chr12:38531400-38531800 Bivalent Enhancer Spleen Spleen
15 chr12:38531400-38532200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood

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