Variant report

Variant rs12468456
Chromosome Location chr2:31501161-31501162
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr2:31482600-31501400 Weak transcription Liver Liver
4 chr2:31486600-31510000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr2:31490000-31502400 Weak transcription Spleen Spleen
6 chr2:31492400-31507800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr2:31492800-31510600 Weak transcription Aorta Aorta
8 chr2:31494400-31505600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:31495800-31509800 Weak transcription Esophagus oesophagus
10 chr2:31497000-31501600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:31497000-31510400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr2:31497200-31502600 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr2:31498600-31502000 Weak transcription Placenta Placenta
14 chr2:31499600-31501600 Weak transcription Right Ventricle heart
15 chr2:31500400-31501600 Enhancers Fetal Heart heart
16 chr2:31500400-31501600 Enhancers Fetal Lung lung
17 chr2:31500600-31501400 Enhancers Fetal Stomach stomach
18 chr2:31500600-31501400 Enhancers HUVEC blood vessel
19 chr2:31501000-31501200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
20 chr2:31501000-31502000 Enhancers Breast Myoepithelial Primary Cells Breast
21 chr2:31501000-31502000 Enhancers Fetal Intestine Large intestine

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