Variant report

Variant rs73492213
Chromosome Location chr13:51872316-51872317
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51853000-51889600 Weak transcription Brain Angular Gyrus brain
2 chr13:51855600-51875400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr13:51867200-51873000 Weak transcription Brain Anterior Caudate brain
4 chr13:51867400-51872800 Weak transcription Fetal Stomach stomach
5 chr13:51867600-51872600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr13:51867600-51910800 Weak transcription Pancreas Pancrea
7 chr13:51870600-51873000 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr13:51871200-51872400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr13:51871600-51872400 Enhancers ES-WA7 Cell Line embryonic stem cell
10 chr13:51871600-51872800 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr13:51871600-51873000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr13:51871800-51872800 Weak transcription H9 Cell Line embryonic stem cell
13 chr13:51871800-51875800 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr13:51871800-51877400 Weak transcription Fetal Brain Female brain
15 chr13:51872000-51873400 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr13:51872000-51875000 Weak transcription HUES48 Cell Line embryonic stem cell
17 chr13:51872000-51875400 Weak transcription HUES64 Cell Line embryonic stem cell
18 chr13:51872200-51876200 Weak transcription ES-I3 Cell Line embryonic stem cell

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