Variant report

Variant rs2024852
Chromosome Location chr6:109819789-109819790
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109813400-109821200 Weak transcription Thymus Thymus
2 chr6:109813400-109823000 Weak transcription HSMM muscle
3 chr6:109815800-109837200 Weak transcription Primary B cells from cord blood blood
4 chr6:109816800-109819800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr6:109817600-109820200 Enhancers H1 Cell Line embryonic stem cell
6 chr6:109817800-109822400 Weak transcription Placenta Placenta
7 chr6:109818200-109823400 Weak transcription HSMMtube muscle
8 chr6:109818400-109823000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:109818400-109823000 Weak transcription Primary T cells from cord blood blood
10 chr6:109818400-109823200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr6:109818800-109819800 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr6:109819200-109819800 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr6:109819200-109820000 Enhancers HUES48 Cell Line embryonic stem cell
14 chr6:109819200-109820000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr6:109819400-109819800 Enhancers HUES64 Cell Line embryonic stem cell
16 chr6:109819600-109820400 Enhancers Fetal Kidney kidney

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