Variant report

Variant rs17598226
Chromosome Location chr4:100496891-100496892
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100495400-100497000 Enhancers HUES64 Cell Line embryonic stem cell
2 chr4:100495600-100497000 Enhancers iPS-15b Cell Line embryonic stem cell
3 chr4:100495600-100497200 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
4 chr4:100495600-100500400 Active TSS Fetal Intestine Large intestine
5 chr4:100495800-100500400 Active TSS Fetal Intestine Small intestine
6 chr4:100495800-100500800 Active TSS Duodenum Mucosa Duodenum
7 chr4:100496000-100497000 Active TSS Fetal Kidney kidney
8 chr4:100496000-100497200 Active TSS Duodenum Smooth Muscle Duodenum
9 chr4:100496000-100497600 Active TSS HepG2 liver
10 chr4:100496200-100497000 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
11 chr4:100496200-100497200 Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr4:100496200-100498200 Active TSS Liver Liver
13 chr4:100496400-100497000 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr4:100496400-100497200 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr4:100496400-100497200 Active TSS Stomach Smooth Muscle stomach
16 chr4:100496600-100497000 Enhancers HUES48 Cell Line embryonic stem cell
17 chr4:100496600-100497000 Enhancers GM12878-XiMat blood
18 chr4:100496800-100497200 Flanking Active TSS Cortex derived primary cultured neurospheres brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links