Variant report

Variant rs12126358
Chromosome Location chr1:212067856-212067857
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:212060000-212068600 Weak transcription A549 lung
2 chr1:212063200-212068600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:212063200-212070200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:212063200-212070200 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr1:212063200-212074600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:212064000-212068600 Enhancers HepG2 liver
7 chr1:212065800-212069400 Enhancers Fetal Intestine Large intestine
8 chr1:212066000-212069600 Enhancers Fetal Intestine Small intestine
9 chr1:212066200-212068800 Weak transcription Pancreas Pancrea
10 chr1:212066800-212070000 Weak transcription Fetal Muscle Leg muscle
11 chr1:212067000-212068600 Weak transcription Liver Liver
12 chr1:212067600-212068200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr1:212067600-212069000 Enhancers Monocytes-CD14+_RO01746 blood
14 chr1:212067600-212069200 Enhancers Primary monocytes fromperipheralblood blood
15 chr1:212067800-212069200 Enhancers Duodenum Mucosa Duodenum

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