| Tag | Content |
|---|
EnhancerAtlas ID | HS050-25917 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr16:57537220-57538270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr16:57538004-57538018 | TGTCCCTTGGGACT | - | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 57537600 | 57537806 | | chr16 | 57537898 | 57538069 |
| Enhancer Sequence | TTGCCGAGGG GTGACAATAG AGCATTAAAC CAAGCCCTGG GCCCTCGGAA GTGTAGGGCC 60
CAAAGTGACA GCACAGGCTG CCCGCACAAC CGTGAAGCTG GCCTTCTTGG CAAGTCTCTT 120
CCTCCCAGAA AAGAGGTCTT GCAGGCGTGG AGCAGCAGAG AGGAGGTAAG CGTGGGAGGC 180
CAGCTCGGGG AGCAGCCCAG CCCAGCCATG GCTCACTGCC GGGTAGCCGG AGAGCCTCTG 240
GGGCCTCCTT GAGGCTGCCT GTCAGGCTGA TGGAGTGGAT AGATGCGGTA GAAGCAGATG 300
GGGCCGGTGA CCTGGCAGAC AGGTGCGCGC ATAACACCTC TGCAGCCACA AAGCCGTGCA 360
AGCCCAGCAT GTGGGAGGGA CTGGCGTGGC AAGGATTTGC TGCCTGCGGA GCGGGAGAAG 420
AAAGCTGAGA TTAACAACAG TGAGAGCAAC AGAAGCTCTT CCTGCACACT CATGGGTGCC 480
AGGTGCTGTG CTTGGCCTGA AGAGCCATCC CTTGAGACTG GAGCCACTGT TACCCCCACT 540
GAGGCCCAGA GGGGAGAAGT GGCAGCATCT AGAAATCCTG AGTCCTCTTC TCTGTTCTTC 600
CTTGTCCACC TCCAGCCCTG TCCTGCAAGG GACCAATGCC TGGAGTGGAT GGGGAACTGG 660
CCACCAGTGG CAAGGGAGAA ACCCAGGAGT CCCACCTCCC AGAATGGGGC TTTGCCTCGA 720
TGTTGGGGGA CCTGTTGCCC CAGTCCCTTG TTGAGCCTCC ACCTTCTCCT CCCTTTACGA 780
AGCCTGTCCC TTGGGACTGA GGGCAGAGGG GTGTGTGTGT GTGTGTGTGT GTATGTGTGT 840
GTGTGTCCTG GATGCATAGG AGCTTCCCCT CCTTCCTCAA GGGAGTCAGC CCCCCCACTG 900
CCAGGACCCA CAGCCAAGGC CAGCTCCATG GCCAGACCCC AGATGTTCCT TCCTGGCGCC 960
TCTGTTACTG TTTTTGAATC AGCCGTGCGG TAGCCCCTCC ACCCTATCTG GGTTTGATCG 1020
TCCATAAAAA AATTAATGGT CCCTGCAAAT 1050
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