| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04441 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:160951100-160952300 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:160951290-160951304 | CCCGCCTCGGCCTC | + | 6.01 |
| | | 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 |
| GH01I160980 | chr1 | 160950786 | 160952753 |
| Enhancer Sequence | TCACATTGTC GCCCAGGCTG GAGTGCAGTG GCCGATCTCG GCTCACTGCA AACTCCGCCT 60
CCCAGGTTCA CGCCATTCTC CTGCCTCAGC CGCCCGCCAC CTTGCCCGGT TAATTTTTTT 120
GTATTTTTAG TAGAGACGGG GTTTCACTGT GGTAGCCAGG ATGGTCTCGA TCCCCTGACC 180
TCGTGATCCC CCCGCCTCGG CCTCCCAAAG TGCTAGGATT ACAGGCGTGA GCCACCGCGC 240
CCAGCCAGTA ATACTTTTTA TAATCCCCTT TCTCTTCTCC CTCATTTTCT CCAATCCCGC 300
TCCCCTAACC CACAGAATCC AGTTGCGCAC CCTAGTTCCC AGGGCGGGTC CCCAGCCCTC 360
GGCTCTTTGC AATGTAAATT AAGTCAGCTT CCCCGTAAAT ACCTTGCGCT GGCCTCTCCC 420
AGGCTTTTCA GTTCTGCCCT TTCTATAATT CTGCATCACA AAAGTTCAGA ACCAGTCTGG 480
CCAGGATCTA CTCTCCCAGA GATGGGAAGT GGGACGCAGT CGCTGCAAGG TATCAGAAAT 540
GGGGTCGGGA CAGGAGGCGC AGCTTGCAGT GAGCCGAGAT AGCGCCACTG CACTCCAGCC 600
TGGGCGAAAA AGCGAGACTC CATTTCAAAA AAAAGAAAAG AAAAGAAAAA AAAAGAAATG 660
GGGTCGGGAA GCCTGGAGGA GGGGACGCGG CGGCGCCCCT GCACTCACCC ACACCTCCAA 720
ACCCTGCGCA GGGAACATCC CCGCGCGTCC CCGCTGCCCC GCTTCAAGCC TAGCGCATGG 780
CTCCTCCCCG TGCCTTGAAG ATGCCACGGG GCTGAGCCAC CTTGCACAAA AAGATTTGGA 840
ACCCACACCT TCTTAGAATC AAGGCCTGGG GATTAAAGCC CCTCCACGAT TAGGTCTTCC 900
GCCCCAAGGG AGAGCAAGAA GACGAGCGGC CACTCGGTGT CCCCCTGAGC CGTATCCAGG 960
GCCACTCGGG GCTCAGCCAG ACCGCGAGGT CTTGGTGTTC GTTCCTCCCT AACTTGGCCG 1020
TGGGGCGGCA CAGCAGGCTT CCTGGCCCCA GCGCTTCCCC TTAGGGCCAG ATTGGCCTCC 1080
GAGTGTAGCA GGACTAGCCA CAGACAAAAC TCCTCAGACA CCGAGTTAAA GAAGGAAGGG 1140
GTTTATTCAG CGAGGGCCAT TGGCAAGACT CCTGTCTCAA GAGCCGAGAT CCCCAAGTGA 1200
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