Variant report

Variant rs17075139
Chromosome Location chr13:51577555-51577556
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51568000-51579800 Weak transcription Pancreas Pancrea
2 chr13:51575400-51578200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr13:51575400-51578400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr13:51575400-51579000 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr13:51575400-51579000 Weak transcription Right Atrium heart
6 chr13:51575400-51579200 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr13:51575400-51580200 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr13:51575600-51578400 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr13:51575600-51578400 Weak transcription Esophagus oesophagus
10 chr13:51575600-51578800 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr13:51575600-51579000 Weak transcription H9 Cell Line embryonic stem cell
12 chr13:51575600-51579200 Weak transcription H1 Cell Line embryonic stem cell
13 chr13:51575600-51579200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr13:51575600-51579800 Weak transcription Aorta Aorta
15 chr13:51576000-51577800 Weak transcription Fetal Muscle Leg muscle
16 chr13:51576000-51579400 Weak transcription Fetal Thymus thymus
17 chr13:51576200-51577800 Weak transcription Brain Germinal Matrix brain
18 chr13:51576600-51578400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr13:51576600-51578400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
20 chr13:51577000-51578200 Weak transcription Fetal Intestine Large intestine
21 chr13:51577000-51578800 Weak transcription Fetal Intestine Small intestine

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