| Tag | Content |
|---|
EnhancerAtlas ID | HS050-25046 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr16:11495730-11496670 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr16:11495754-11495768 | AGTCCCTTGGGGAT | - | 6.39 | | Nr5a2 | MA0505.1 | chr16:11496570-11496585 | GCTGACCTTGAACAT | - | 7.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGCCCCCCC AGTGCCTTTC CCACAGTCCC TTGGGGATGT GGTACAGCCT CATTGACCCC 60
AGATAAGGCT CCTCAGGCAG GGGAGGGCCC CAAAGACCCC GCTCAGCCTG CAGGGTGGAG 120
TTCAGCTCTG CCCCAGGGTC ACCTTCCGGC CCTGACACTT ACCTGGTCCC TGCCATCCCA 180
GCCGACAACC AGGCCATCCC GGTGGCTGCC TCCCAAATGC TCTGAGGACA GGCGGAGGCT 240
GCAGTGTCGC GGCAGGGGGA GGGGCAGCGG GTGGGTGAGC TCCACTGGGT GGGTGAGGAC 300
ACACACAAAG GGTAGGGCAC GTGAGCTGAG GTCAGCAGCT CCAGGCCCAA GGGGGTTCAG 360
GGGACTCAAC TGACGCCACT GCCAGCTCAC GCAAATGGCC ACTCGGGGGC CACACAGCCA 420
GATAATTTTC ACAAAACTCA GAAGCTACAC ACTCGCTTTG TCACCATTAC CACTCGACAC 480
CCTGCACTGT CCCTGTGGGA GCCCCGTTAC AATGAGACTC TGAGGCTCCT CCAAGAGGTG 540
GCGTCTGCCT CCCCAGCCCT TGAAGCTGGG CTGGCCTCGT GACGTGCTAA TAAAATTCAG 600
CAAAGTTGAC CGAGTGCCAG TTCTAAGCCC AGGCCTTAGG AGGCCTCACC CCGCTTCCTC 660
CCTTGAACCC CTGTCCAGCC ACATGAGAAC AAACCCTGCT GGCCTGTGGG CTGGTGCCAC 720
GTGGGGTTGG GGAGAGCCTG CTTTCAGCTC AGGATGTCCT AGCGCAGCTG ACAGCTAGCC 780
AGCCCCTGAG CAGGCTGGAG AGCCCAGCCA AGGCCAGCGG AGCCGCCCGC TCACCCTACA 840
GCTGACCTTG AACATGAGGA AGACCAGAAA AGCTGCCCAG GTGACCCACA GCCTCGTGAG 900
CAAGGCGCCA CGCTTGCTTT ATGCCGCTGA GTTTCGGAAT 940
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