Variant report

Variant rs9487128
Chromosome Location chr6:109818706-109818707
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109812800-109819000 Weak transcription Fetal Kidney kidney
2 chr6:109813400-109821200 Weak transcription Thymus Thymus
3 chr6:109813400-109823000 Weak transcription HSMM muscle
4 chr6:109815800-109837200 Weak transcription Primary B cells from cord blood blood
5 chr6:109816400-109819200 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr6:109816400-109819400 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr6:109816800-109819200 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr6:109816800-109819800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr6:109817600-109820200 Enhancers H1 Cell Line embryonic stem cell
10 chr6:109817800-109822400 Weak transcription Placenta Placenta
11 chr6:109818200-109823400 Weak transcription HSMMtube muscle
12 chr6:109818400-109818800 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr6:109818400-109819200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr6:109818400-109823000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:109818400-109823000 Weak transcription Primary T cells from cord blood blood
16 chr6:109818400-109823200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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