Variant report

Variant rs6541155
Chromosome Location chr1:220839702-220839703
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220791200-220841200 Weak transcription HMEC breast
2 chr1:220828800-220839800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:220829400-220847200 Weak transcription Right Ventricle heart
4 chr1:220829600-220845800 Weak transcription Fetal Heart heart
5 chr1:220830600-220840200 Weak transcription Fetal Brain Male brain
6 chr1:220831400-220845800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:220835600-220839800 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr1:220835600-220840000 Weak transcription H9 Cell Line embryonic stem cell
9 chr1:220835600-220840800 Weak transcription Fetal Brain Female brain
10 chr1:220836200-220842800 Weak transcription Adipose Nuclei Adipose
11 chr1:220836600-220840000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:220838200-220840400 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr1:220839400-220840000 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr1:220839400-220840200 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr1:220839600-220839800 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr1:220839600-220839800 Enhancers HUES48 Cell Line embryonic stem cell
17 chr1:220839600-220839800 Enhancers HUES64 Cell Line embryonic stem cell
18 chr1:220839600-220840000 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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