| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00067 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:1473920-1475060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr1:1474564-1474575 | AATGACCTTGA | - | 6.32 | | Esrra | MA0592.2 | chr1:1474565-1474576 | ATGACCTTGAG | - | 6.02 | | Esrrg | MA0643.1 | chr1:1474565-1474575 | ATGACCTTGA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1474111 | 1474179 | | chr1 | 1474237 | 1474365 |
| Enhancer Sequence | GTGGAGCCGA CCTCAGGCCT TTGCTCAGCA GTCGGACCTG CCAGCCAGGG ACACGGGGCT 60
CTCTGGTAGC ATGTGGCCAC CCCACAAGCT CTTACCCCCT ACCCTGTGCC CAGCACACGT 120
GAGGGTCACA GACACCCCGA TCTCTGCCTT CTCTAACACC CGTGTTCTTC ATCGACACGC 180
CTGCTGCACC CATAGGCATG TCACACGCTT AGCAACACAT GCAGCTGTCC TGAACACACA 240
TGCCCCACAC CCACACGTAT GCACAGAGAC CCCCGGAGCA GGAGGCAGCA GAGATGACGA 300
ACACGGGTTC TGGGCTGGTG CCCCCTTTGT CCTTCACTAG CTGTGTGACC TTGGAAAAGC 360
CTGTCCTCTA AATCCTCCGT CCACTTCCTC ATCTGTTCAG CAGGGTTAAC AGCGGCCACT 420
GCGTGAGGGT GTCCTGAGGG GTGGAAGTGC ATGCGTGCGT GCGCGGGGGC TGTGTGTACG 480
CACATGTATA TGCACAGACG CCACACACAT GCGCGTCTCA TGAGAAGATG TTTATTTCGT 540
ACATGGACGT ACAAACATGC ATGGCCAAGA GGATCCCATC GCTACACGTG CACAGAGGGG 600
GTCACACGGT GGGTGCGGGG GGTCTGGGCG CTCCCCTCAA TCTGAATGAC CTTGAGGAAG 660
CTCCACCTCC CCGCTGCCCC CCCAGCCCAT CCCTCAGCTC CTCTCCAGCC CGGGGGTGGT 720
GCCCAGTGCC CCTCAAGGCA GGCCCTTCCC GCCTTGACCT GCATTCCCCT GCCCAGGGAC 780
TCAGTGCAGG GCCCAGCCCT GTGCCAGCAG GCGCTTCCTG CCCCAGCCCT GATGAGGCTG 840
GCTTGGGTCT CCACTGTGGA CATCACACTG GGCTGCGGCT TTCCGGCCTC CAGGCTGGAC 900
CAGGAGGCCC CGTGACCCAT TCCGCCATCA CCCTGGAGGC CTCTAGGAAC GGCGTCCTAA 960
AGCCATGCGC CCCCAGGAGA CCCCCGCCCA CCTTGAGACA GCTCCTCCCC CTGCGCACCT 1020
GGCAGCCCTC AAGGGTGGAA GGCGGCTCGC GGCCTGCGTG GGGCTGGTTC CCCCGCGCCC 1080
CGAGTGGGCC CCGCCACACA TGTGCGCTCA CGCGTGTCGA GCCGGCGCCG GTTGTGGACT 1140
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