| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70664 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr9:132004720-132006190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr9:132005828-132005849 | ATCAGTGCCTGGGACAGTGCC | + | 6.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 132005480 | 132005830 | | chr9 | 132005135 | 132005862 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH09I129242 | chr9 | 132004868 | 132005869 |
| Enhancer Sequence | CATGCTGGTT GGGAGGGGAA CTGGAAGAGT GGGCTTCATT CCACGTATAG GGGGAGCCCC 60
AAAGAGTCTG TAGCCAAGGA AGTGACAGGG TCTGATTTGC TTTTAGAGGA TCTCTGAGGC 120
TACTGGGAGG AGAAGGCGTG GAGCTGGGTG AGAATGGAGG CAGGGAGGCC TAGGAGGGGC 180
TGGCGGTGAT GAGGCTGGGG TTGAGGAGGA GGCCGCAGGA AGGGAGACAA AGGGAGGCAT 240
TTGGAAAGCA TCCAGAAGTC GCGTGGCTGG GACCTGATAA CAGGTGTGAG CCAGGGGCTG 300
AGAGGCAGGG AGGACTTAAG GTATGCAAGG ACAGCTGAGG GAGGATGGGT GTCATTCGCA 360
GATTGGAGGA GCCCTGGAGG AGGAGCCAGT CTGGCTGGGG TGCAGGAGGG CAGGGTGACA 420
AAGATCCAGT TTTGGCCAAG GTGCCTTTGG GTCATGAGTG GGGACATGCA GTGTCTGTGA 480
GGGTGGCTGG GATTTCGGGG CAGCCATGAT CCAGTCGAAG CCCTTCCCCA GCCCCTGGCC 540
TCCAGCAAAA TCAGGACTTG GGGCCTGTTC CTTGGGGCCT CGGGAACACG CAGATCTCAT 600
TCCCCGCCCC AGTTTCTCTG GAAGGAAAAC ACCCAGGGCC TCGGTGGAAC CGGCATTAAT 660
TTCCCCTGTT CGGCTCATCA TTCCATCATC ACGAGAGAGC CAAACAGATG ACCATTTCGT 720
CATTGCATAT GCCCATGCGG GGCTTCCGTA ATCTGATCAC TTAATCACAT GCTTATTCCA 780
TGAGGACGGA GGCACGGGCA AGCTCTGGGG CCCACTCCTT GGGCAGCGCA TTTTGGACCA 840
AGTCCCTTAG CGTTCCTGGC TGCCTCTGTT TCTCTGCCTG CCTTGGGAAT CCAGACAGCC 900
TCATGACAAG AGGAGATGAG GCAGTGGTTG CGGAAGAGCC TGGTCTCTCA GCCACAGCAG 960
CCACGAGGTG CTGGCAAGCT CTCTGCAGCC TGTGCTGCTG GGAGGTAGAG GCTTCGGCAG 1020
CTTGTCCTCC TTGTGGCCTA ACACACGCTG CCCGTCTCCC CACTTGCATG GAAGCCCCAG 1080
GAGGACACGC AGTTTGTCTC TTTGGTTCAT CAGTGCCTGG GACAGTGCCT GGCACATGAG 1140
GGAGCTTAGG TGAAGTTTAT CGAAATTTCC CATTTGTCTT TTTGTTTTGT TTTGTTTTTA 1200
AGACAGTGTC TCGCTCTGTC GCCAAGGCTG GAGTTCAGTG GTGTGATCTC AACTCACTGC 1260
AACCTCCGCC TCCTGGATTC AAGCAATTCT CTGCCTCAGC CTCCCAAGTA GTTGGGACTA 1320
CAGACACACG CCACCACACC CAGCTAATTT TTTTTTTTAA GAGATGGGGG TTGTACCATG 1380
TTGGCCAGGC TGGTCTTGAA CTCCTGGCCT CAAGTGATCC ACCTGCCTTG GCCTCCCAAA 1440
GTGCTAGGAT TACAGGCATG AGCCACCAAG 1470
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