Variant report

Variant rs10177050
Chromosome Location chr2:31500884-31500885
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31463600-31501400 Weak transcription Pancreas Pancrea
2 chr2:31468200-31501600 Weak transcription Primary hematopoietic stem cells blood
3 chr2:31482000-31501000 Weak transcription Fetal Intestine Large intestine
4 chr2:31482600-31501400 Weak transcription Liver Liver
5 chr2:31486600-31510000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr2:31490000-31502400 Weak transcription Spleen Spleen
7 chr2:31492400-31507800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:31492800-31510600 Weak transcription Aorta Aorta
9 chr2:31494400-31505600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:31495800-31509800 Weak transcription Esophagus oesophagus
11 chr2:31497000-31501600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr2:31497000-31510400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr2:31497200-31502600 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr2:31497400-31501000 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr2:31498600-31502000 Weak transcription Placenta Placenta
16 chr2:31499600-31501600 Weak transcription Right Ventricle heart
17 chr2:31500400-31501600 Enhancers Fetal Heart heart
18 chr2:31500400-31501600 Enhancers Fetal Lung lung
19 chr2:31500600-31501400 Enhancers Fetal Stomach stomach
20 chr2:31500600-31501400 Enhancers HUVEC blood vessel

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