Variant report

Variant rs74139762
Chromosome Location chr1:220716483-220716484
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220703400-220724400 Weak transcription Aorta Aorta
2 chr1:220706000-220723800 Weak transcription Fetal Brain Male brain
3 chr1:220708800-220718000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:220710200-220717800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:220715400-220717600 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr1:220715600-220718600 Enhancers HUES48 Cell Line embryonic stem cell
7 chr1:220715800-220716800 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr1:220716000-220718200 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr1:220716000-220722400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr1:220716200-220716600 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr1:220716200-220717200 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr1:220716200-220717200 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr1:220716200-220717200 Weak transcription iPS-20b Cell Line embryonic stem cell

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