Variant report

Variant rs12022213
Chromosome Location chr1:113983654-113983655
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:113940200-113987000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:113966800-113986600 Weak transcription Fetal Intestine Small intestine
3 chr1:113970000-113986600 Weak transcription Esophagus oesophagus
4 chr1:113981000-113986600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:113981000-113986600 Weak transcription Aorta Aorta
6 chr1:113981200-113986800 Weak transcription Psoas Muscle Psoas
7 chr1:113981400-113986600 Weak transcription H1 Cell Line embryonic stem cell
8 chr1:113981400-113986800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr1:113981600-113983800 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr1:113981800-113986800 Weak transcription Pancreas Pancrea
11 chr1:113982000-113983800 Weak transcription Gastric stomach
12 chr1:113982200-113983800 Enhancers A549 lung
13 chr1:113982200-113986600 Weak transcription Sigmoid Colon Sigmoid Colon
14 chr1:113982200-113987400 Weak transcription Fetal Intestine Large intestine
15 chr1:113983200-113984000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr1:113983400-113984000 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr1:113983400-113985000 Enhancers HUES48 Cell Line embryonic stem cell
18 chr1:113983600-113985000 Enhancers iPS-18 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links