Variant report

Variant rs62248962
Chromosome Location chr3:42936739-42936740
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:42929000-42937200 Weak transcription H9 Cell Line embryonic stem cell
2 chr3:42931000-42937800 Weak transcription Placenta Placenta
3 chr3:42933200-42938200 Enhancers Stomach Mucosa stomach
4 chr3:42933800-42941800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:42934000-42936800 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr3:42934000-42937600 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr3:42934000-42937600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr3:42935800-42937800 Enhancers HepG2 liver
9 chr3:42936000-42937000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr3:42936000-42937000 Enhancers Fetal Intestine Large intestine
11 chr3:42936600-42937000 Enhancers Placenta Amnion Placenta Amnion
12 chr3:42936600-42937400 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr3:42936600-42937400 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr3:42936600-42937800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr3:42936600-42937800 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr3:42936600-42940000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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