| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70868 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:135114850-135116290 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:135115012-135115032 | CTGGGGCTGGTGTGTGGGGG | - | 6.03 |
|
| | 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 |
| GH09I132239 | chr9 | 135115121 | 135115270 |
|
Enhancer Sequence | CCCTTGCGGT TCTCCGGTAA GTTTTGCACT GGAGTTGCAA AACTTACCAG TGGCCCTTCC 60
CTCTCTGGGC AACTGGAGGG GACACTGACC CTTCCTGGCT CCAAAGAGCT GTGACTCTGG 120
CAGGTGGCAG GCACTCAGTG GCAGAGGCCA CTGAGCATCT GTCTGGGGCT GGTGTGTGGG 180
GGGGTCCCCC TCCATAGCTC CTTTCCAGAA AGGTGGAGGA GCAGCCTATC CCTCCTCCTG 240
CAGGGGCCCA GTTGGGGGCC AAAAGATCGC CTTGCTGCGT GCATTTGTGC AAGTCCCTTC 300
CCGTTCCTGG GCCTCAGCTT CCTCATTCAT CAAATTGGGA GGCAGATCAG ATCAAAGGTT 360
TTCAGCTCTT TTTTGTGGCT GAAGCTTTTC TTCAAATGCT TTACCAGCCC AGGTCCAGCT 420
ATAAAGCTGC TCTTCACCCC TGGTGGGCAC CCAGTCTGCT TTCTTCCAAG TTCTACTCAA 480
GGACTGGCTT TTGGGTAGAG AAGGAAGTCC ATCAGGGCCC TGGGCCTGGG CAAAGACCAA 540
AGCCATGACC GCCAACCAAA ACGCACCAGC CTGGAATGGT TGCCCCTGTC GTCAGTAGAG 600
GCCAGGTCTC GGCCTCAGGG GCTGTCCCCC AACCCTGCCC AGCCAGGCCC CTTGGGACAC 660
CATCACCCAT CCCCCACCCA GCAGGAGGCT CTGGCTGCCC AGAGGAGGGG CTCCTGCAAA 720
GCTGGAGCTG TCGGTCTGAA TTCTGGCGGC AGCCTTCAGA TAATTCCATC AACTCTAAGT 780
GATCAAAGCC GCTGACGTCA CAGGGGGCCA GCTGCAGGGA CAGGGCAGGG CCTTTGGATC 840
CAATTAGAGG TGCCCACACC CTGGCACCCT CCTCCTCTCC CTGGCTCTCC CTGCCTCCAC 900
CCCGAGAGCC AGCACTGAGC TGCAAGGTTT CTCAGGGTGG ACGATATTCA CCCTCTCCCA 960
CAGAGCCCCA AGGCAACCAA CTGGGCCCAC CCCGGGAGCA GGAATAGGCT GTTCCTCCAC 1020
TCCCCTGCAA AGGAGCTATG GAGGGGGGCC ACCCCACAAC ACAGCAGCCC CAGACATGCT 1080
CAGTGGCCTC TGCTGAGTTT CTGCCACCTG TCGGAGTCAT AGCTCTTTGG AGATGGGAAG 1140
GACAGCGACC CCTCTAGTTG CCCAGAGAGG GGAAGGGGCT GACCCAGGCC ACACCAGTGC 1200
CAGGGCGGGG AAGGTGGGGC TGGGACGTGT TTGATCCCAA GGAAGGAAGC CAGAGTCTTC 1260
TCTCCAGGCC TGGCCACCCT GGGAAGTCCC CACCTGCCGT CCAGCCGCGG GCTCACGTGG 1320
ACCCAGTGTG GGGAGCATCC CCTGGGGAGT GTGGAGATGC TCCCTGCGAG GCCGGGAGAG 1380
TGGGGGTCCG AGAAGACGGC GCCCACACGT AGCCCTGACC GCGCGCCCGT GCCCGTGTCC 1440
|
