Variant report

Variant rs1406898
Chromosome Location chr6:109824440-109824441
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109815800-109837200 Weak transcription Primary B cells from cord blood blood
2 chr6:109819800-109824800 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr6:109819800-109828200 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr6:109819800-109828200 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr6:109820200-109824600 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr6:109820200-109824800 Weak transcription H1 Cell Line embryonic stem cell
7 chr6:109820400-109824800 Weak transcription Fetal Kidney kidney
8 chr6:109822400-109826000 Enhancers Placenta Placenta
9 chr6:109823000-109825000 Enhancers HSMM muscle
10 chr6:109823400-109824800 Weak transcription Muscle Satellite Cultured Cells --
11 chr6:109823400-109834600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr6:109823800-109828200 Weak transcription Primary T cells from cord blood blood
13 chr6:109824000-109824600 Enhancers Pancreatic Islets Pancreatic Islet
14 chr6:109824000-109825000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr6:109824000-109825400 Enhancers Fetal Muscle Leg muscle
16 chr6:109824400-109825200 Enhancers HSMMtube muscle
17 chr6:109824400-109825400 Enhancers Liver Liver
18 chr6:109824400-109826200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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