| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69298 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:94609470-94610630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr9:94609726-94609739 | TTCATTTGCATAC | + | 6.21 | | Pou2f3 | MA0627.1 | chr9:94609725-94609741 | CTTCATTTGCATACCA | - | 6.6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I091847 | chr9 | 94609813 | 94610748 |
|
Enhancer Sequence | AAGGCATCAG TATGTGCAGG TCTGCAGACA GCACAGACAG ACTTAGAACC AGAAAGACGG 60
GAGAAGTGCC TGTCCCACTG GACAGAAAGC CTGACCCCTC TGGGAGGCCA CTTTCCCTCC 120
CTCCTGGACC CCTCATTAGG CCTCGCTACC ATCTCCCCAA ATTCCAGAGG TAGTCCTTTG 180
CAGACAAGAT CTACTGCCAG GTCCCTCGAC GCCCCCTTGC TCCTCTGTAC AAGGCACCAA 240
AACATGGGAA GCAGGCTTCA TTTGCATACC ACACATATAC TCCCCCAGAA AGGGCTCCCT 300
AATGCAGTCC CCCCACTTCC CACATAAAGA GACTTGAGGG CGCCAGAGGA GGCCCTGCAG 360
GAGCCAGCTC ATACAGCAAC AGTTCCAGTC TTTCAAAGTA AGCCCAGGCA GGCGGGACCC 420
AACTGCACCC CAGCTCTCCT CCAGAGCCGC TTTTCTCATT TCCGTGTGCA GCCTGCCAGG 480
GCTGAGGGTC GAGAGCAGGC CTGAGAATGA ACCCCACTCC CAGCACATGA TGGATCCTGC 540
CCTTGCCGGC CAGGAGATGC TGGTCGCAGG AAGACATCCT TCACGTCTTC GCTGCCACCA 600
AGAATCACAC TCCCCAGAAC TCAAGTTCCG CTCGACCAAG CTCAAGTCAG GCTTTGATCT 660
TGCAGGAAAC ACCCACGCAG ACTCACTCTC CAGGACGGGA AGGATGCAGG AGCCAGCTTC 720
AGCAGAACTC CTGGCTAGCA GCTCTGCCTG GCAGTACAGA AACTGTCTCA AAATGTGAAA 780
CAGATGAGCC TTTTAAAGAA AGTTATTTAT ATTGTGGAAT CTTTCAGAGC AAGCAGAAAC 840
TTGAAGAGCC TTATCACCTG GGGCACAAAA CCAAGGATAC TCGAGTCTTC TCTCACCATG 900
GAAATGGATG TGATTTTACC AAAACATAAC AAGGAAATAT GTTGGTTTGA TGCTATTTCT 960
TGATTTCTAC TTCTGATAAC GTATGCATGC CAGTCCTAAT CAAGACAGAA TGCCATTCAA 1020
TAAGCTGACA AAGAACTCTT TTCCTGCGAA TCCCCTACCT TGAAGGTCAG TATTAACAGT 1080
GAAGCATGGA AATTAAATTA AATTAAACCA GGGGAGCGGA GCTGTATGTA AACTCTGCTG 1140
GTTTTTCAGA AAAGGAGTGG 1160
|
