| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70779 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:133374970-133376360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr9:133376167-133376180 | GATAAATTAATTA | - | 6.11 | | SOX10 | MA0442.2 | chr9:133376336-133376347 | TTCTTTGTTTT | - | 6.62 | | Sox3 | MA0514.1 | chr9:133375311-133375321 | CCTTTGTTTT | + | 6.02 | | ZNF263 | MA0528.1 | chr9:133375992-133376013 | CCCTCCGTCACCTCCACCTCC | - | 6.18 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33497 | chr9:133371778-133378014 | H2171 |
|
| | 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 |
| GH09I130497 | chr9 | 133372415 | 133377081 |
|
Enhancer Sequence | GGCCCTGACG GGCCTTCAGA GCCTCCAGGT GTAAAGGGTA GGCTTTGAGA GCCCCCAGGT 60
GTAAAGGGTA GGCTTTGATG CGACCTTGAC TGCTGCCCTG CCCTGCCCTG CCCTGCCCTA 120
GACAAACCCC ACTTTCCTGT CCATCTGCCC ATAGCATCCT CAGAAGCATG CTTTGATAGC 180
CGACAGTAAC AGAGGGTCCT AGGCATTGGG GTCCTAGGTT CCTGTGTCCC ACCGGGTGCC 240
TCTGATACTT GCCCTCCCCT CCCGCTAAGC CACAGGGACT CCACTATGAG CTCCTTTGCA 300
GGGCAGGTTA AACAAGGAAA TAGCATAGAG GTGGAGAGAA GCCTTTGTTT TCTGTCACCA 360
TACCTGAGCT GTAGGTCTAG CTGGAAGCCA TCCTAGCCAC GTGGATCTCC ATGGCCCAGG 420
AGGGTGGTGC ACGTCATCTG AAGTCACTCA GACCTTTGAT CCTCTGTGAG TCACCAGTAA 480
GAGTGTCAGC TGTACCTGCC TCACAGATGC AGTGAAGGTT CAATATGAGC CTGTGGAAAT 540
CAAGCATGCG GCTCAGGCTT AGACCCTGGC ATGCAGGAAG AGCCAGGGGC AGTGCCAGCA 600
GCAAGCACAC TCAGCCCAGG GCCGGTGTGC TCAAGGGCAA ACAGGGTCGT TTGTCACCAG 660
CAGCTAACAT AGACTAAGCT GCTCTGGGAC ACTCTCCTAG GATGTCTCAT TTAATTCTTA 720
CACAAAATTT GCAACTCCCC GGGAACAGGC TGAGTGGTTA AGTAACTTTC CAAGGGTCAC 780
ACAGCTAGGA GGTGGTGGAG CTGAGTCCGG AGGGCCTGTC CTGCTGTGGG TTCTCCATCA 840
CCAGCTCCCT TCTCATGGGG ATTGGAGTCT AGAAGAAGAT GCAAGTCAGT CTCCTCTTGC 900
TAACAACATG CCCTGGGCAC AGAGCCATCA TTTTCTCCCA GAGCCAGTCT CTTGTCCCTG 960
GAGGCACCTC ATGCCCCGAG AGATGTTGAA GCCCGCCCAT CTGCCCAGGG TCCTCTCCCT 1020
TCCCCTCCGT CACCTCCACC TCCCCTGCCT CCTGCGCCCT CTGTTTGTAT TTTATGACTC 1080
TATAAACCCT TTTAAATGGC CCAGAACAAA CAGGGCTTAC ATAGTGGCCT CTTCATTTCT 1140
CCTATTGCCA GTTAAACGCT TTGTCTTCAA CAATGACAAA CAATGTTTTC CCCCTAAGAT 1200
AAATTAATTA CATTATCCTG ATTGGAGGGC AGGAGGGGCC AGGGCGGGAG AGGGAATAGA 1260
AAAAAAGGCA ACTTCACACA CATCTTAACA AACAGCTGCC CCAGCCACCC CAGCTCTGCC 1320
TGAATTAATT GAACCCAGTG TGTGTTGTTA TTGTTAATTT ACATTTTTCT TTGTTTTGAA 1380
TCTGGTTTAC 1390
|
