Variant report

Variant rs4805112
Chromosome Location chr19:35686954-35686955
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:35684800-35687800 Enhancers Liver Liver
2 chr19:35685200-35688600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr19:35685400-35691800 Weak transcription Primary T helper cells fromperipheralblood blood
4 chr19:35685600-35690000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
5 chr19:35685600-35693800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr19:35685800-35687000 Weak transcription K562 blood
7 chr19:35685800-35689600 Weak transcription Primary T cells fromperipheralblood blood
8 chr19:35685800-35691800 Weak transcription Primary T helper cells PMA-I stimulated --
9 chr19:35686200-35687800 Enhancers NHDF-Ad bronchial
10 chr19:35686600-35687000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr19:35686600-35687600 Enhancers Fetal Intestine Small intestine
12 chr19:35686600-35687800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr19:35686600-35687800 Enhancers Fetal Intestine Large intestine
14 chr19:35686800-35687200 Enhancers HepG2 liver

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